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Chapter 6<br />

<strong>Clinical</strong> Veterinary Immunology<br />

Laurel J. Gershwin<br />

Department <strong>of</strong> Pathology, Microbiology, and Immunology<br />

School <strong>of</strong> Veterinary Medicine<br />

University <strong>of</strong> California, Davis<br />

Davis, California<br />

I. INTRODUCTION<br />

II. INNATE IMMUNITY<br />

III. ACQUIRED IMMUNITY<br />

A. Humoral Immunity<br />

B. Cellular Immunity<br />

IV. EVALUATION OF THE IMMUNE RESPONSE<br />

A. Evaluation <strong>of</strong> Neutrophil Function<br />

B. Evaluation <strong>of</strong> Complement<br />

C. Evaluation <strong>of</strong> Humoral Immunity<br />

D. Evaluation <strong>of</strong> Cellular Immunity<br />

V. METHODS FOR EVALUATION OF THE IMMUNE<br />

RESPONSE TO INFECTIOUS AGENTS<br />

A. Agglutination and Passive Agglutination<br />

B. Hemagglutination and Hemagglutination-<br />

Inhibition<br />

C. Virus Serum Neutralization Assay<br />

D. Agar Gel Double Immunodiffusion<br />

E. Indirect and Direct Immun<strong>of</strong>luorescence (IFA) Test<br />

F. Flow Cytometry<br />

G. Enzyme-Linked Immunosorbent Assay (ELISA)<br />

H. Immunohistochemistry/Immunoperoxidase<br />

Techniques<br />

I. Western Blot Analysis<br />

J. How Do the Sensitivities <strong>of</strong> Different Immunoassays<br />

Compare<br />

K. Interpretation <strong>of</strong> Immune Responses to<br />

Pathogens<br />

VI. LABORATORY DIAGNOSIS OF DISEASES WITH AN<br />

IMMUNOLOGICAL PATHOGENESIS<br />

A. Autoimmune Diseases<br />

B. Primary Immune Deficiency Diseases<br />

C. Secondary Immunodeficiency<br />

D. Hypersensitivity Diseases<br />

VII. MODULATION OF THE IMMUNE RESPONSE<br />

VIII. SUMMARY<br />

REFERENCES<br />

I . INTRODUCTION<br />

The field <strong>of</strong> clinical immunology has evolved from serological<br />

testing for the presence <strong>of</strong> antibodies to infectious agents<br />

to a multifaceted discipline that utilizes some <strong>of</strong> the traditional<br />

techniques in addition to many newer more sensitive<br />

assay systems. Yet it is still involved with evaluation <strong>of</strong> the<br />

immune system <strong>of</strong> patients and the ability <strong>of</strong> the immune<br />

system to respond to antigenic stimuli. Assays developed to<br />

target specific parts <strong>of</strong> the immune system enable the clinician<br />

not only to determine if a patient has normal immune<br />

responsiveness but also to target those parts <strong>of</strong> the immune<br />

system that are suspect <strong>of</strong> inadequate function. Serology<br />

has historically been used to determine retrospectively if a<br />

patient were infected with a particular disease agent; antibody<br />

titers continue to have importance in diagnostics.<br />

Current technologies have created expanded opportunities<br />

to diagnose infectious, autoimmune, and allergic<br />

diseases with new tools. Diagnostic quantitative reverse transcriptase<br />

polymerase chain reaction (RT-PCR) has shifted<br />

the focus from the immunology laboratory for the identification<br />

<strong>of</strong> infecting pathogens. Yet growing concern that<br />

veterinarians may be overvaccinating their patients has provided<br />

a new incentive for the development <strong>of</strong> sensitive and<br />

specific immunoassays to measure the immune response<br />

to vaccine antigens. Another increasing trend since the<br />

previous edition <strong>of</strong> this book is the use <strong>of</strong> diagnostic flow<br />

cytometry. This technique can evaluate multiple parameters<br />

on cells using multicolor analysis. The current availability<br />

<strong>of</strong> antibodies to many cytokines makes it now possible to<br />

determine not only cell phenotype but also the intracellular<br />

cytokines being made. Production <strong>of</strong> monoclonal antibodies<br />

specific to some leukocyte antigens expressed on<br />

leukemic cells has allowed diagnosis <strong>of</strong> these conditions to<br />

be achieved through flow cytometry. Flow cytometry is currently<br />

being used for detection <strong>of</strong> autoantibodies to platelets<br />

and erythrocytes. The traditional antinuclear antibody<br />

<strong>Clinical</strong> <strong>Biochemistry</strong> <strong>of</strong> <strong>Domestic</strong> <strong>Animals</strong>, 6th <strong>Edition</strong> 157<br />

Copyright © 2008, Elsevier Inc.<br />

All rights reserved.

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