8536d_ch01_001-023 8/1/02 4:25 PM Page 1 mac79 Mac 79:45_BW:Goldsby et al. / Immunology 5e: chapter 1 Overview of the Immune System T        defense system that has evolved to protect animals from invading pathogenic microorganisms and cancer.It is able to generate an enormous variety ofcells and molecules capable of specifically recognizing and eliminat- ing an apparently limitless variety offoreign invaders.These cells and molecules act together in a dynamic network whose complexity rivals that ofthe nervous system. Functionally, an immune response can be divided into Numerous T Lymphocytes Interacting with a Single two related activities—recognition and response.Immune Macrophage recognition is remarkable for its specificity. The immune system is able to recognize subtle chemical differences that distinguish one foreign pathogen from another. Further- (cid:2) Historical Perspective more, the system is able to discriminate between foreign (cid:2) Innate Immunity molecules and the body’s own cells and proteins.Once a for- eign organism has been recognized, the immune system (cid:2) Adaptive Immunity recruits a variety ofcells and molecules to mount an appro- (cid:2) Comparative Immunity priate response,called an effector response,to eliminate or neutralize the organism. In this way the system is able to (cid:2) Immune Dysfunction and Its Consequences convert the initial recognition event into a variety ofeffector responses,each uniquely suited for eliminating a particular type ofpathogen.Later exposure to the same foreign organ- ism induces a memory response, characterized by a more rapid and heightened immune reaction that serves to elimi- Like the later chapters covering basic topics in immu- nate the pathogen and prevent disease. nology, this one includes a section called “Clinical Focus” This chapter introduces the study of immunology from that describes human disease and its relation to immunity. an historical perspective and presents a broad overview of These sections investigate the causes,consequences,or treat- the cells and molecules that compose the immune system, ments ofdiseases rooted in impaired or hyperactive immune along with the mechanisms they use to protect the body function. against foreign invaders.Evidence for the presence of very simple immune systems in certain invertebrate organisms then gives an evolutionary perspective on the mammalian Historical Perspective immune system,which is the major subject ofthis book.El- ements of the primitive immune system persist in verte- The discipline of immunology grew out of the observation brates as innate immunityalong with a more highly evolved that individuals who had recovered from certain infectious system of specific responses termed adaptive immunity. diseases were thereafter protected from the disease. The These two systems work in concert to provide a high degree Latin term immunis,meaning “exempt,”is the source ofthe ofprotection for vertebrate species.Finally,in some circum- English word immunity, meaning the state of protection stances,the immune system fails to act as protector because from infectious disease. of some deficiency in its components;at other times,it be- Perhaps the earliest written reference to the phenomenon comes an aggressor and turns its awesome powers against its ofimmunity can be traced back to Thucydides,the great his- own host. In this introductory chapter, our description of torian of the Peloponnesian War.In describing a plague in immunity is simplified to reveal the essential structures and Athens,he wrote in 430 BCthat only those who had recov- function ofthe immune system.Substantive discussions,ex- ered from the plague could nurse the sick because they perimental approaches,and in-depth definitions are left to would not contract the disease a second time.Although early the chapters that follow. societies recognized the phenomenon of immunity,almost 8536d_ch01_001-023 8/1/02 4:25 PM Page 2 mac79 Mac 79:45_BW:Goldsby et al. / Immunology 5e: 2 PART I Introduction two thousand years passed before the concept was success- fully converted into medically effective practice. The first recorded attempts to induce immunity deliber- ately were performed by the Chinese and Turks in the fif- teenth century.Various reports suggest that the dried crusts derived from smallpox pustules were either inhaled into the nostrils or inserted into small cuts in the skin (a technique called variolation).In 1718,Lady Mary Wortley Montagu,the wife of the British ambassador to Constantinople,observed the positive effects of variolation on the native population and had the technique performed on her own children.The method was significantly improved by the English physician Edward Jenner,in 1798.Intrigued by the fact that milkmaids who had contracted the mild disease cowpox were subse- quently immune to smallpox,which is a disfiguring and of- ten fatal disease,Jenner reasoned that introducing fluid from a cowpox pustule into people (i.e.,inoculating them) might protect them from smallpox.To test this idea,he inoculated an eight-year-old boy with fluid from a cowpox pustule and later intentionally infected the child with smallpox.As pre- dicted,the child did not develop smallpox. Jenner’s technique ofinoculating with cowpox to protect against smallpox spread quickly throughout Europe. How- ever, for many reasons, including a lack of obvious disease targets and knowledge of their causes,it was nearly a hun- dred years before this technique was applied to other dis- eases. As so often happens in science, serendipity in combination with astute observation led to the next major advance in immunology, the induction of immunity to FIGURE 1-1 Wood engraving of Louis Pasteur watching Joseph cholera. Louis Pasteur had succeeded in growing the bac- Meister receive the rabies vaccine. [From Harper’s Weekly 29:836; terium thought to cause fowl cholera in culture and then had courtesy of the National Library of Medicine.] shown that chickens injected with the cultured bacterium de- veloped cholera.After returning from a summer vacation,he injected some chickens with an old culture.The chickens be- 1885, Pasteur administered his first vaccine to a human, a came ill, but, to Pasteur’s surprise, they recovered. Pasteur young boy who had been bitten repeatedly by a rabid dog then grew a fresh culture ofthe bacterium with the intention (Figure 1-1).The boy,Joseph Meister,was inoculated with a ofinjecting it into some fresh chickens.But,as the story goes, series of attenuated rabies virus preparations.He lived and his supply ofchickens was limited,and therefore he used the later became a custodian at the Pasteur Institute. previously injected chickens.Again to his surprise,the chick- ens were completely protected from the disease. Pasteur Early Studies Revealed Humoral and Cellular hypothesized and proved that aging had weakened the viru- Components of the Immune System lence of the pathogen and that such an attenuated strain might be administered to protect against the disease. He Although Pasteur proved that vaccination worked,he did not called this attenuated strain a vaccine(from the Latin vacca, understand how. The experimental work of Emil von meaning “cow”), in honor of Jenner’s work with cowpox Behring and Shibasaburo Kitasato in 1890 gave the first in- inoculation. sights into the mechanism ofimmunity,earning von Behring Pasteur extended these findings to other diseases,demon- the Nobel prize in medicine in 1901 (Table 1-1).Von Behring strating that it was possible to attenuate, or weaken, a and Kitasato demonstrated that serum(the liquid,noncellu- pathogen and administer the attenuated strain as a vaccine. lar component ofcoagulated blood) from animals previously In a now classic experiment at Pouilly-le-Fort in 1881,Pas- immunized to diphtheria could transfer the immune state to teur first vaccinated one group ofsheep with heat-attenuated unimmunized animals.In search ofthe protective agent,var- anthrax bacillus (Bacillus anthracis);he then challenged the ious researchers during the next decade demonstrated that vaccinated sheep and some unvaccinated sheep with a viru- an active component from immune serum could neutralize lent culture ofthe bacillus.All the vaccinated sheep lived,and toxins,precipitate toxins,and agglutinate (clump) bacteria. all the unvaccinated animals died. These experiments In each case,the active agent was named for the activity it ex- marked the beginnings of the discipline of immunology.In hibited: antitoxin, precipitin, and agglutinin, respectively. 8536d_ch01_001-023 8/1/02 4:25 PM Page 3 mac79 Mac 79:45_BW:Goldsby et al. / Immunology 5e: Overview of the Immune System CHAPTER 1 3 TABLE 1-1 Nobel Prizes for immunologic research Year Recipient Country Research 1901 Emil von Behring Germany Serum antitoxins 1905 Robert Koch Germany Cellular immunity to tuberculosis 1908 Elie Metchnikoff Russia Role of phagocytosis (Metchnikoff) and Paul Ehrlich Germany antitoxins (Ehrlich) in immunity 1913 Charles Richet France Anaphylaxis 1919 Jules Border Belgium Complement-mediated bacteriolysis 1930 Karl Landsteiner United States Discovery of human blood groups 1951 Max Theiler South Africa Development of yellow fever vaccine 1957 Daniel Bovet Switzerland Antihistamines 1960 F. Macfarlane Burnet Australia Discovery of acquired immunological Peter Medawar Great Britain tolerance 1972 Rodney R. Porter Great Britain Chemical structure of antibodies Gerald M. Edelman United States 1977 Rosalyn R. Yalow United States Development of radioimmunoassay 1980 George Snell United States Major histocompatibility complex Jean Daussct France Baruj Benacerraf United States 1984 Cesar Milstein Great Britain Monoclonal antibody Georges E. Köhler Germany Niels K. Jerne Denmark Immune regulatory theories 1987 Susumu Tonegawa Japan Gene rearrangement in antibody production 1991 E. Donnall Thomas United States Transplantation immunology Joseph Murray United States 1996 Peter C. Doherty Australia Role of major histocompatibility complex Rolf M. Zinkernagel Switzerland in antigen recognition by by T cells Initially,a different serum component was thought to be re- In due course, a controversy developed between those sponsible for each activity, but during the 1930s, mainly who held to the concept of humoral immunity and those through the efforts of Elvin Kabat,a fraction of serum first who agreed with Metchnikoff’s concept ofcell-mediated im- called gamma-globulin (now immunoglobulin) was shown munity.It was later shown that both are correct—immunity to be responsible for all these activities.The active molecules requires both cellular and humoral responses.It was difficult in the immunoglobulin fraction are called antibodies. Be- to study the activities of immune cells before the develop- cause immunity was mediated by antibodies contained in ment of modern tissue culture techniques,whereas studies body fluids (known at the time as humors),it was called hu- with serum took advantage ofthe ready availability ofblood moral immunity. and established biochemical techniques. Because of these In 1883,even before the discovery that a serum compo- technical problems, information about cellular immunity nent could transfer immunity, Elie Metchnikoff demon- lagged behind findings that concerned humoral immunity. strated that cells also contribute to the immune state of an In a key experiment in the 1940s,Merrill Chase succeeded animal.He observed that certain white blood cells,which he in transferring immunity against the tuberculosis organism termed phagocytes, were able to ingest (phagocytose) mi- by transferring white blood cells between guinea pigs.This croorganisms and other foreign material.Noting that these demonstration helped to rekindle interest in cellular immu- phagocytic cells were more active in animals that had been nity.With the emergence ofimproved cell culture techniques immunized,Metchnikoffhypothesized that cells,rather than in the 1950s, the lymphocyte was identified as the cell re- serum components, were the major effector of immunity. sponsible for both cellular and humoral immunity. Soon The active phagocytic cells identified by Metchnikoff were thereafter, experiments with chickens pioneered by Bruce likely blood monocytes and neutrophils (see Chapter 2). Glick at Mississippi State University indicated that there were 8536d_ch01_001-023 8/1/02 4:25 PM Page 4 mac79 Mac 79:45_BW:Goldsby et al. / Immunology 5e: 4 PART I Introduction two types of lymphocytes:T lymphocytes derived from the In the 1930s and 1940s, the selective theory was chal- thymus mediated cellular immunity, and B lymphocytes lenged by various instructional theories, in which antigen from the bursa of Fabricius (an outgrowth of the cloaca in played a central role in determining the specificity ofthe an- birds) were involved in humoral immunity.The controversy tibody molecule.According to the instructional theories, a about the roles of humoral and cellular immunity was re- particular antigen would serve as a template around which solved when the two systems were shown to be intertwined, antibody would fold.The antibody molecule would thereby and that both systems were necessary for the immune assume a configuration complementary to that ofthe antigen response. template. This concept was first postulated by Friedrich Breinl and Felix Haurowitz about 1930 and redefined in the Early Theories Attempted to Explain 1940s in terms of protein folding by Linus Pauling.The in- the Specificity of the Antibody– structional theories were formally disproved in the 1960s,by which time information was emerging about the structure of Antigen Interaction DNA,RNA,and protein that would offer new insights into One ofthe greatest enigmas facing early immunologists was the vexing problem of how an individual could make anti- the specificity ofthe antibody molecule for foreign material, bodies against almost anything. or antigen(the general term for a substance that binds with In the 1950s, selective theories resurfaced as a result of a specific antibody).Around 1900,Jules Bordet at the Pasteur new experimental data and, through the insights of Niels Institute expanded the concept ofimmunity by demonstrat- Jerne, David Talmadge, and F. Macfarlane Burnet, were re- ing specific immune reactivity to nonpathogenic substances, fined into a theory that came to be known as the clonal- such as red blood cells from other species.Serum from an an- selection theory. According to this theory, an individual imal inoculated previously with material that did not cause lymphocyte expresses membrane receptors that are specific infection would react with this material in a specific manner, for a distinct antigen.This unique receptor specificity is de- and this reactivity could be passed to other animals by trans- termined before the lymphocyte is exposed to the antigen. ferring serum from the first.The work of Karl Landsteiner Binding of antigen to its specific receptor activates the cell, and those who followed him showed that injecting an animal causing it to proliferate into a clone of cells that have the with almost any organic chemical could induce production same immunologic specificity as the parent cell.The clonal- of antibodies that would bind specifically to the chemical. selection theory has been further refined and is now accepted These studies demonstrated that antibodies have a capacity as the underlying paradigm ofmodern immunology. for an almost unlimited range of reactivity, including re- sponses to compounds that had only recently been synthe- The Immune System Includes Innate and sized in the laboratory and had not previously existed in Adaptive Components nature.In addition,it was shown that molecules differing in the smallest detail could be distinguished by their reactivity Immunity—the state of protection from infectious disease with different antibodies.Two major theories were proposed —has both a less specific and more specific component.The to account for this specificity:the selective theory and the in- less specific component,innate immunity,provides the first structional theory. line ofdefense against infection.Most components ofinnate The earliest conception ofthe selective theorydates to Paul immunity are present before the onset ofinfection and con- Ehrlich in 1900.In an attempt to explain the origin ofserum stitute a set of disease-resistance mechanisms that are not antibody,Ehrlich proposed that cells in the blood expressed a specific to a particular pathogen but that include cellular and variety of receptors,which he called “side-chain receptors,” molecular components that recognize classes of molecules that could react with infectious agents and inactivate them. peculiar to frequently encountered pathogens. Phagocytic Borrowing a concept used by Emil Fischer in 1894 to explain cells,such as macrophages and neutrophils,barriers such as the interaction between an enzyme and its substrate,Ehrlich skin,and a variety ofantimicrobial compounds synthesized proposed that binding ofthe receptor to an infectious agent by the host all play important roles in innate immunity.In was like the fit between a lock and key.Ehrlich suggested that contrast to the broad reactivity of the innate immune sys- interaction between an infectious agent and a cell-bound tem,which is uniform in all members of a species,the spe- receptor would induce the cell to produce and release more cific component, adaptive immunity, does not come into receptors with the same specificity. According to Ehrlich’s play until there is an antigenic challenge to the organism. theory,the specificity ofthe receptor was determined before Adaptive immunity responds to the challenge with a high de- its exposure to antigen,and the antigen selected the appro- gree of specificity as well as the remarkable property of priate receptor. Ultimately all aspects of Ehrlich’s theory “memory.”Typically,there is an adaptive immune response would be proven correct with the minor exception that the against an antigen within five or six days after the initial ex- “receptor”exists as both a soluble antibody molecule and as a posure to that antigen.Exposure to the same antigen some cell-bound receptor; it is the soluble form that is secreted time in the future results in a memory response:the immune rather than the bound form released. response to the second challenge occurs more quickly than 8536d_ch01_001-023 8/1/02 4:25 PM Page 5 mac79 Mac 79:45_BW:Goldsby et al. / Immunology 5e: Overview of the Immune System CHAPTER 1 5 the first,is stronger,and is often more effective in neutraliz- distinct layers:a thinner outer layer—the epidermis—and a ing and clearing the pathogen.The major agents ofadaptive thicker layer—the dermis. The epidermis contains several immunity are lymphocytes and the antibodies and other layers of tightly packed epithelial cells.The outer epidermal molecules they produce. layer consists ofdead cells and is filled with a waterproofing Because adaptive immune responses require some time to protein called keratin. The dermis, which is composed of marshal,innate immunity provides the first line of defense connective tissue,contains blood vessels,hair follicles,seba- during the critical period just after the host’s exposure to a ceous glands,and sweat glands.The sebaceous glands are as- pathogen.In general,most of the microorganisms encoun- sociated with the hair follicles and produce an oily secretion tered by a healthy individual are readily cleared within a few called sebum.Sebum consists of lactic acid and fatty acids, days by defense mechanisms of the innate immune system which maintain the pH ofthe skin between 3 and 5;this pH before they activate the adaptive immune system. inhibits the growth ofmost microorganisms.A few bacteria that metabolize sebum live as commensals on the skin and sometimes cause a severe form of acne. One acne drug, Innate Immunity isotretinoin (Accutane), is a vitamin A derivative that pre- vents the formation ofsebum. Innate immunity can be seen to comprise four types of de- Breaks in the skin resulting from scratches, wounds, or fensive barriers: anatomic, physiologic, phagocytic, and in- abrasion are obvious routes of infection.The skin may also flammatory (Table 1-2). be penetrated by biting insects (e.g.,mosquitoes,mites,ticks, fleas, and sandflies); if these harbor pathogenic organisms, The Skin and the Mucosal Surfaces Provide they can introduce the pathogen into the body as they feed. The protozoan that causes malaria,for example,is deposited Protective Barriers Against Infection in humans by mosquitoes when they take a blood meal.Sim- Physical and anatomic barriers that tend to prevent the entry ilarly,bubonic plague is spread by the bite offleas,and Lyme ofpathogens are an organism’s first line ofdefense against in- disease is spread by the bite ofticks. fection.The skin and the surface ofmucous membranes are The conjunctivae and the alimentary, respiratory, and included in this category because they are effective barriers to urogenital tracts are lined by mucous membranes,not by the the entry ofmost microorganisms.The skin consists oftwo dry,protective skin that covers the exterior ofthe body.These TABLE 1-2 Summary of nonspecific host defenses Type Mechanism Anatomic barriers Skin Mechanical barrier retards entry of microbes. Acidic environment (pH 3–5) retards growth of microbes. Mucous membranes Normal flora compete with microbes for attachment sites and nutrients. Mucus entraps foreign microorganisms. Cilia propel microorganisms out of body. Physiologic barriers Temperature Normal body temperature inhibits growth of some pathogens. Fever response inhibits growth of some pathogens. Low pH Acidity of stomach contents kills most ingested microorganisms. Chemical mediators Lysozyme cleaves bacterial cell wall. Interferon induces antiviral state in uninfected cells. Complement lyses microorganisms or facilitates phagocytosis. Toll-like receptors recognize microbial molecules, signal cell to secrete immunostimulatory cytokines. Collectins disrupt cell wall of pathogen. Phagocytic/endocytic barriers Various cells internalize (endocytose) and break down foreign macromolecules. Specialized cells (blood monocytes, neutrophils, tissue macrophages) internalize (phagocytose), kill, and digest whole microorganisms. Inflammatory barriers Tissue damage and infection induce leakage of vascular fluid, containing serum proteins with antibacterial activity, and influx of phagocytic cells into the affected area. 8536d_ch01_001-023 8/1/02 4:25 PM Page 6 mac79 Mac 79:45_BW:Goldsby et al. / Immunology 5e: 6 PART I Introduction membranes consist ofan outer epithelial layer and an under- tissues are susceptible to bacterial invasion, whereas others lying layer of connective tissue. Although many pathogens are not. enter the body by binding to and penetrating mucous mem- branes,a number ofnonspecific defense mechanisms tend to Physiologic Barriers to Infection Include prevent this entry.For example,saliva,tears,and mucous se- General Conditions and Specific Molecules cretions act to wash away potential invaders and also contain antibacterial or antiviral substances.The viscous fluid called The physiologic barriers that contribute to innate immu- mucus,which is secreted by epithelial cells ofmucous mem- nity include temperature,pH,and various soluble and cell- branes,entraps foreign microorganisms.In the lower respi- associated molecules.Many species are not susceptible to cer- ratory tract, the mucous membrane is covered by cilia, tain diseases simply because their normal body temperature hairlike protrusions of the epithelial-cell membranes. The inhibits growth of the pathogens. Chickens, for example, synchronous movement of cilia propels mucus-entrapped have innate immunity to anthrax because their high body microorganisms from these tracts. In addition, nonpatho- temperature inhibits the growth ofthe bacteria.Gastric acid- genic organisms tend to colonize the epithelial cells of mu- ity is an innate physiologic barrier to infection because very cosal surfaces. These normal flora generally outcompete few ingested microorganisms can survive the low pH of the pathogens for attachment sites on the epithelial cell surface stomach contents. One reason newborns are susceptible to and for necessary nutrients. some diseases that do not afflict adults is that their stomach Some organisms have evolved ways ofescaping these de- contents are less acid than those ofadults. fense mechanisms and thus are able to invade the body A variety of soluble factors contribute to innate immu- through mucous membranes. For example, influenza virus nity,among them the soluble proteins lysozyme,interferon, (the agent that causes flu) has a surface molecule that enables and complement.Lysozyme, a hydrolytic enzyme found in it to attach firmly to cells in mucous membranes ofthe respi- mucous secretions and in tears,is able to cleave the peptido- ratory tract,preventing the virus from being swept out by the glycan layer ofthe bacterial cell wall.Interferoncomprises a ciliated epithelial cells. Similarly, the organism that causes group of proteins produced by virus-infected cells.Among gonorrhea has surface projections that allow it to bind to ep- the many functions ofthe interferons is the ability to bind to ithelial cells in the mucous membrane ofthe urogenital tract. nearby cells and induce a generalized antiviral state.Comple- Adherence ofbacteria to mucous membranes is due to inter- ment,examined in detail in Chapter 13,is a group ofserum actions between hairlike protrusions on a bacterium,called proteins that circulate in an inactive state.A variety of spe- fimbriaeor pili,and certain glycoproteins or glycolipids that cific and nonspecific immunologic mechanisms can convert are expressed only by epithelial cells of the mucous mem- the inactive forms of complement proteins into an active brane ofparticular tissues (Figure 1-2).For this reason,some state with the ability to damage the membranes of patho- genic organisms,either destroying the pathogens or facilitat- ing their clearance.Complement may function as an effector system that is triggered by binding of antibodies to certain cell surfaces, or it may be activated by reactions between complement molecules and certain components ofmicrobial cell walls.Reactions between complement molecules or frag- ments ofcomplement molecules and cellular receptors trig- ger activation of cells of the innate or adaptive immune systems.Recent studies on collectinsindicate that these sur- factant proteins may kill certain bacteria directly by disrupt- ing their lipid membranes or,alternatively,by aggregating the bacteria to enhance their susceptibility to phagocytosis. Many of the molecules involved in innate immunity have the property ofpattern recognition,the ability to recognize a given class ofmolecules.Because there are certain types ofmol- ecules that are unique to microbes and never found in multi- cellular organisms, the ability to immediately recognize and combat invaders displaying such molecules is a strong feature ofinnate immunity.Molecules with pattern recognition ability may be soluble, like lysozyme and the complement compo- FIGURE 1-2 Electron micrograph of rod-shaped Escherichia coli nents described above,or they may be cell-associated receptors. bacteria adhering to surface of epithelial cells of the urinary tract. Among the class ofreceptors designated the toll-like receptors [From N. Sharon and H. Lis, 1993, Sci. Am. 268(1):85; photograph (TLRs),TLR2 recognizes the lipopolysaccharide (LPS) found courtesy of K. Fujita.] on Gram-negative bacteria.It has long been recognized that 8536d_ch01_007 9/5/02 11:47 AM Page 7 mac46 mac46:385_reb: Overview of the Immune System CHAPTER 1 7 FIGURE 1-3 (a) Electronmicrograph of macrophage (pink) attack- (a) ing Escherichia coli (green). The bacteria are phagocytized as de- scribed in part b and breakdown products secreted. The monocyte (purple) has been recruited to the vicinity of the encounter by soluble factors secreted by the macrophage. The red sphere is an erythrocyte. (b) Schematic diagram of the steps in phagocytosis of a bacterium. [Part a, Dennis Kunkel Microscopy, Inc./Dennis Kunkel.] systemic exposure ofmammals to relatively small quantities of purified LPS leads to an acute inflammatory response (see be- low). The mechanism for this response is via a TLR on macrophages that recognizes LPS and elicits a variety ofmole- cules in the inflammatory response upon exposure.When the TLR is exposed to the LPS upon local invasion by a Gram-neg- ative bacterium,the contained response results in elimination ofthe bacterial challenge. (b) Cells That Ingest and Destroy Pathogens Make Up a Phagocytic Barrier to Infection 1 Bacterium becomes attached Another important innate defense mechanism is the inges- to membrane evaginations called pseudopodia tion of extracellular particulate material by phagocytosis. Phagocytosis is one type ofendocytosis,the general term for 2 the uptake by a cell of material from its environment. In Bacterium is ingested, phagocytosis,a cell’s plasma membrane expands around the forming phagosome particulate material, which may include whole pathogenic microorganisms, to form large vesicles called phagosomes 3 (Figure 1-3).Most phagocytosis is conducted by specialized Phagosome fuses with lysosome cells, such as blood monocytes, neutrophils, and tissue macrophages (see Chapter 2).Most cell types are capable of other forms of endocytosis,such as receptor-mediated endo- 4 Lysosomal enzymes digest cytosis,in which extracellular molecules are internalized after captured material binding by specific cellular receptors, and pinocytosis, the process by which cells take up fluid from the surrounding 5 medium along with any molecules contained in it. Digestion products are released from cell Inflammation Represents a Complex Sequence of Events That Stimulates Immune Responses Tissue damage caused by a wound or by an invading patho- of inflammation” as rubor (redness), tumor (swelling), genic microorganism induces a complex sequence of events calor(heat),and dolor(pain).In the second century AD,an- collectively known as the inflammatory response. As de- other physician,Galen,added a fifth sign:functio laesa(loss scribed above,a molecular component ofa microbe,such as offunction).The cardinal signs ofinflammation reflect the LPS,may trigger an inflammatory response via interaction three major events ofan inflammatory response (Figure 1-4): with cell surface receptors.The end result of inflammation may be the marshalling ofa specific immune response to the 1. Vasodilation—an increase in the diameter ofblood invasion or clearance of the invader by components of the vessels—ofnearby capillaries occurs as the vessels that innate immune system. Many of the classic features of the carry blood away from the affected area constrict, inflammatory response were described as early as 1600 BC,in resulting in engorgement ofthe capillary network.The Egyptian papyrus writings. In the first century AD, the engorged capillaries are responsible for tissue redness Roman physician Celsus described the “four cardinal signs (erythema) and an increase in tissue temperature. 8536d_ch01_001-023 8/1/02 4:25 PM Page 8 mac79 Mac 79:45_BW:Goldsby et al. / Immunology 5e: 8 PART I Introduction Tissue damage Bacteria 1 4 Tissue damage causes release of Phagocytes and antibacterial vasoactive and chemotactic factors exudate destroy bacteria that trigger a local increase in blood flow and capillary permeability Exudate 3 2 Phagocytes migrate to site of Permeable capillaries allow an (complement, antibody, inflammation (chemotaxis) influx of fluid (exudate) and cells C-reactive protein) Margination Extravasation Capillary FIGURE 1-4 Major events in the inflammatory response. A bacte- blood cells, including phagocytes and lymphocytes, from the blood rial infection causes tissue damage with release of various vasoactive into the tissues. The serum proteins contained in the exudate have and chemotactic factors. These factors induce increased blood flow antibacterial properties, and the phagocytes begin to engulf the bac- to the area, increased capillary permeability, and an influx of white teria, as illustrated in Figure 1-3. 2. An increase in capillary permeabilityfacilitates an influx isms,some are released from damaged cells in response to tis- offluid and cells from the engorged capillaries into the sue injury,some are generated by several plasma enzyme sys- tissue.The fluid that accumulates (exudate)has a much tems, and some are products of various white blood cells higher protein content than fluid normally released from participating in the inflammatory response. the vasculature.Accumulation ofexudate contributes to Among the chemical mediators released in response to tis- tissue swelling (edema). sue damage are various serum proteins called acute-phase proteins.The concentrations ofthese proteins increase dra- 3. Influx ofphagocytesfrom the capillaries into the tissues is matically in tissue-damaging infections.C-reactive protein is facilitated by the increased permeability ofthe capil- a major acute-phase protein produced by the liver in re- laries.The emigration ofphagocytes is a multistep sponse to tissue damage.Its name derives from its pattern- process that includes adherence ofthe cells to the recognition activity: C-reactive protein binds to the endothelial wall ofthe blood vessels (margination), C-polysaccharide cell-wall component found on a variety of followed by their emigration between the capillary- bacteria and fungi. This binding activates the complement endothelial cells into the tissue (diapedesis orextrava- system,resulting in increased clearance of the pathogen ei- sation),and,finally,their migration through the tissue to ther by complement-mediated lysis or by a complement- the site ofthe invasion (chemotaxis).As phagocytic cells mediated increase in phagocytosis. accumulate at the site and begin to phagocytose bacteria, One of the principal mediators of the inflammatory re- they release lytic enzymes,which can damage nearby sponse is histamine,a chemical released by a variety ofcells healthy cells.The accumulation ofdead cells,digested in response to tissue injury.Histamine binds to receptors on material,and fluid forms a substance called pus. nearby capillaries and venules,causing vasodilation and in- The events in the inflammatory response are initiated by a creased permeability. Another important group of inflam- complex series ofevents involving a variety ofchemical me- matory mediators,small peptides called kinins,are normally diators whose interactions are only partly understood.Some present in blood plasma in an inactive form.Tissue injury ac- of these mediators are derived from invading microorgan- tivates these peptides,which then cause vasodilation and in- 8536d_ch01_001-023 8/1/02 4:25 PM Page 9 mac79 Mac 79:45_BW:Goldsby et al. / Immunology 5e: Overview of the Immune System CHAPTER 1 9 creased permeability ofcapillaries.A particular kinin,called sponses are intimately involved in activating the specific im- bradykinin,also stimulates pain receptors in the skin.This mune response.Conversely,various soluble factors produced effect probably serves a protective role, because pain nor- by a specific immune response have been shown to augment mally causes an individual to protect the injured area. the activity ofthese phagocytic cells.As an inflammatory re- Vasodilation and the increase in capillary permeability in sponse develops, for example, soluble mediators are pro- an injured tissue also enable enzymes of the blood-clotting duced that attract cells ofthe immune system.The immune system to enter the tissue.These enzymes activate an enzyme response will,in turn,serve to regulate the intensity ofthe in- cascade that results in the deposition ofinsoluble strands of flammatory response.Through the carefully regulated inter- fibrin,which is the main component ofa blood clot.The fib- play ofadaptive and innate immunity,the two systems work rin strands wall offthe injured area from the rest ofthe body together to eliminate a foreign invader. and serve to prevent the spread ofinfection. Once the inflammatory response has subsided and most The Adaptive Immune System Requires ofthe debris has been cleared away by phagocytic cells,tissue Cooperation Between Lymphocytes and repair and regeneration of new tissue begins. Capillaries Antigen-Presenting Cells grow into the fibrin of a blood clot.New connective tissue cells,called fibroblasts,replace the fibrin as the clot dissolves. An effective immune response involves two major groups of As fibroblasts and capillaries accumulate,scar tissue forms. cells: T lymphocytes and antigen-presenting cells. Lympho- The inflammatory response is described in more detail in cytes are one ofmany types ofwhite blood cells produced in Chapter 15. the bone marrow by the process ofhematopoiesis (see Chap- ter 2).Lymphocytes leave the bone marrow,circulate in the blood and lymphatic systems, and reside in various lym- phoid organs. Because they produce and display antigen- Adaptive Immunity binding cell-surface receptors, lymphocytes mediate the Adaptive immunity is capable ofrecognizing and selectively defining immunologic attributes of specificity, diversity, eliminating specific foreign microorganisms and molecules memory,and self/nonselfrecognition.The two major popu- (i.e., foreign antigens). Unlike innate immune responses, lations oflymphocytes—B lymphocytes (B cells)and T lym- adaptive immune responses are not the same in all members phocytes (T cells)—are described briefly here and in greater ofa species but are reactions to specific antigenic challenges. detail in later chapters. Adaptive immunity displays four characteristic attributes: (cid:2) Antigenic specificity B LYMPHOCYTES B lymphocytes mature within the bone marrow;when they (cid:2) Diversity leave it,each expresses a unique antigen-binding receptor on (cid:2) Immunologic memory its membrane (Figure 1-5a).This antigen-binding or B-cell receptor is a membrane-bound antibody molecule. Anti- (cid:2) Self/nonselfrecognition bodies are glycoproteins that consist of two identical heavy The antigenic specificityofthe immune system permits it to polypeptide chains and two identical light polypeptide distinguish subtle differences among antigens. Antibodies chains.Each heavy chain is joined with a light chain by disul- can distinguish between two protein molecules that differ in fide bonds,and additional disulfide bonds hold the two pairs only a single amino acid.The immune system is capable of together.The amino-terminal ends ofthe pairs ofheavy and generating tremendous diversityin its recognition molecules, light chains form a cleft within which antigen binds.When a allowing it to recognize billions ofunique structures on for- naive B cell (one that has not previously encountered anti- eign antigens.Once the immune system has recognized and gen) first encounters the antigen that matches its membrane- responded to an antigen, it exhibits immunologic memory; bound antibody,the binding of the antigen to the antibody that is,a second encounter with the same antigen induces a causes the cell to divide rapidly;its progeny differentiate into heightened state of immune reactivity. Because of this at- memory B cells and effector B cells called plasma cells. tribute,the immune system can confer life-long immunity to Memory B cells have a longer life span than naive cells,and many infectious agents after an initial encounter.Finally,the they express the same membrane-bound antibody as their immune system normally responds only to foreign antigens, parent B cell. Plasma cells produce the antibody in a form indicating that it is capable of self/nonself recognition. The that can be secreted and have little or no membrane-bound ability ofthe immune system to distinguish selffrom nonself antibody.Although plasma cells live for only a few days,they and respond only to nonselfmolecules is essential,for,as de- secrete enormous amounts of antibody during this time. scribed below,the outcome of an inappropriate response to It has been estimated that a single plasma cell can secrete selfmolecules can be fatal. more than 2000 molecules ofantibody per second.Secreted Adaptive immunity is not independent of innate immu- antibodies are the major effector molecules of humoral nity.The phagocytic cells crucial to nonspecific immune re- immunity. 8536d_ch01_001-023 8/1/02 4:25 PM Page 10 mac79 Mac 79:45_BW:Goldsby et al. / Immunology 5e: 10 PART I Introduction (a) B cell (b) TH cell (c) TC cell TCR CD4 TCR CD8 Antigen- binding receptor (antibody) FIGURE 1-5 Distinctive membrane molecules on lymphocytes. (a) antigen associated with class I MHC molecules. In general, CD4+ B cells have about 105molecules of membrane-bound antibody per cells act as helper cells and CD8+cells act as cytotoxic cells. Both cell. All the antibody molecules on a given B cell have the same anti- types of T cells express about 105identical molecules of the antigen- genic specificity and can interact directly with antigen. (b) T cells binding T-cell receptor (TCR) per cell, all with the same antigenic bearing CD4(CD4+cells) recognize only antigen bound to class II specificity. MHC molecules. (c) T cells bearing CD8(CD8+cells) recognize only T LYMPHOCYTES an important role in activating B cells,T cells,macrophages, C and various other cells that participate in the immune re- T lymphocytes also arise in the bone marrow.Unlike B cells, sponse.Differences in the pattern of cytokines produced by which mature within the bone marrow,T cells migrate to the activated T cells result in different types of immune thymus gland to mature.During its maturation within the H response. thymus,the T cell comes to express a unique antigen-binding Under the influence of T -derived cytokines, a T cell molecule,called the T-cell receptor,on its membrane.Unlike H C that recognizes an antigen–MHC class I molecule complex membrane-bound antibodies on B cells,which can recognize proliferates and differentiates into an effector cell called a cy- antigen alone, T-cell receptors can recognize only antigen totoxic T lymphocyte (CTL).In contrast to the T cell,the that is bound to cell-membrane proteins called major histo- C CTL generally does not secrete many cytokines and instead compatibility complex (MHC) molecules.MHC molecules exhibits cell-killing or cytotoxic activity.The CTL has a vital that function in this recognition event,which is termed “anti- function in monitoring the cells ofthe body and eliminating gen presentation,”are polymorphic (genetically diverse) gly- any that display antigen,such as virus-infected cells,tumor coproteins found on cell membranes (see Chapter 7).There cells,and cells ofa foreign tissue graft.Cells that display for- are two major types ofMHC molecules:Class I MHC mole- eign antigen complexed with a class I MHC molecule are cules,which are expressed by nearly all nucleated cells ofver- called altered self-cells;these are targets ofCTLs. tebrate species, consist of a heavy chain linked to a small invariant protein called (cid:2) -microglobulin. Class II MHC 2 ANTIGEN-PRESENTING CELLS molecules,which consist ofan alpha and a beta glycoprotein chain,are expressed only by antigen-presenting cells.When a Activation of both the humoral and cell-mediated branches naive T cell encounters antigen combined with a MHC mol- of the immune system requires cytokines produced by T H ecule on a cell,the T cell proliferates and differentiates into cells.It is essential that activation of T cells themselves be H memory T cells and various effector T cells. carefully regulated,because an inappropriate T-cell response There are two well-defined subpopulations of T cells: T to self-components can have fatal autoimmune conse- helper (T )and T cytotoxic (T ) cells.Although a third type quences.To ensure carefully regulated activation ofT cells, H C H ofT cell,called a T suppressor (T ) cell,has been postulated, they can recognize only antigen that is displayed together S recent evidence suggests that it may not be distinct from T with class MHC II molecules on the surface ofantigen-pre- H and T subpopulations.T helper and T cytotoxic cells can be senting cells (APCs). These specialized cells, which include C distinguished from one another by the presence of either macrophages,B lymphocytes,and dendritic cells,are distin- CD4or CD8membrane glycoproteins on their surfaces (Fig- guished by two properties: (1) they express class II MHC ure 1-5b,c).T cells displaying CD4 generally function as T molecules on their membranes, and (2) they are able to H cells,whereas those displaying CD8 generally function as T deliver a co-stimulatory signal that is necessary for T -cell C H cells (see Chapter 2). activation. After a T cell recognizes and interacts with an anti- Antigen-presenting cells first internalize antigen,either by H gen–MHC class II molecule complex,the cell is activated—it phagocytosis or by endocytosis, and then display a part of becomes an effector cell that secretes various growth factors that antigen on their membrane bound to a class II MHC known collectively as cytokines.The secreted cytokines play molecule. The T cell recognizes and interacts with the H