Foot-and-Mouth Disease Virus Can Induce a Specific and Rapid CD4 + T-Cell-Independent Neutralizing and Isotype Class-Switched Antibody Response in Naïve Cattle

Author:

Juleff Nicholas12,Windsor Miriam1,Lefevre Eric A.3,Gubbins Simon1,Hamblin Pip1,Reid Elizabeth1,McLaughlin Kerry1,Beverley Peter C. L.4,Morrison Ivan W.2,Charleston Bryan1

Affiliation:

1. Pirbright Laboratory, Institute for Animal Health, Ash Road, Woking, Surrey GU24 0NF, United Kingdom

2. Centre for Tropical Veterinary Medicine, University of Edinburgh, Easter Bush Veterinary Centre, Roslin, Midlothian EH25 9RG, United Kingdom

3. Compton Laboratory, Institute for Animal Health, Compton, Newbury, Berkshire RG20 7NN, United Kingdom

4. the Edward Jenner Institute for Vaccine Research, University of Oxford, Compton, Newbury, Berkshire RG20 7NN, United Kingdom

Abstract

ABSTRACT The role of T-lymphocyte subsets in recovery from foot-and-mouth disease virus (FMDV) infection in calves was investigated by administering subset-specific monoclonal antibodies. The depletion of circulating CD4 + or WC1 + γδ T cells was achieved for a period extending from before challenge to after resolution of viremia and peak clinical signs, whereas CD8 + cell depletion was only partial. The depletion of CD4 + cells was also confirmed by analysis of lymph node biopsy specimens 5 days postchallenge. Depletion with anti-WC1 and anti-CD8 antibodies had no effect on the kinetics of infection, clinical signs, and immune responses following FMDV infection. Three of the four CD4 + T-cell-depleted calves failed to generate an antibody response to the nonstructural polyprotein 3ABC but generated a neutralizing antibody response similar to that in the controls, including rapid isotype switching to immunoglobulin G antibody. We conclude that antibody responses to sites on the surface of the virus capsid are T cell independent, whereas those directed against the nonstructural proteins are T cell dependent. CD4 depletion was found to substantially inhibit antibody responses to the G-H peptide loop VP1 135-156 on the viral capsid, indicating that responses to this particular site, which has a more mobile structure than other neutralizing sites on the virus capsid, are T cell dependent. The depletion of CD4 + T cells had no adverse effect on the magnitude or duration of clinical signs or clearance of virus from the circulation. Overall, we conclude that CD4 + T-cell-independent antibody responses play a major role in the resolution of foot-and-mouth disease in cattle.

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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