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B cells and antibody response in calves primary-infected or re-infected with Cooperia oncophora: influence of priming dose and host responder types

Research output: Contribution to journalArticle

  • K Kanobana
  • A Koets
  • FNJ Kooyman
  • N Bakker
  • HW Ploeger
  • L Vervelde

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Original languageEnglish
Pages (from-to)1487-1502
Number of pages16
JournalInternational Journal For Parasitology
Volume33
Issue number13
DOIs
Publication statusPublished - Nov 2003

Abstract

We investigated whether the generation of protective memory humoral immunity in Cooperia oncophoro infected calves occurs in a dose-dependent way and whether it depends on the animal responder types. To this end, serum and mucus antibody responses were measured in animals primary-infected with 30,000 or 100,000 L3, treated with anthelmintics and subsequently challenged with 100,000 L3. A detailed phenotypic and functional analysis of B cells was done in animals infected once or twice with 100,000 L3. Based on the similarity in parasitological variables of animals primed with 30,000 or 100,000 L3, we concluded that with these doses priming conferred protection in a dose-independent way. Upon challenge significant increases in Cooperia-specific serum and mucus IgG1 and IgA and total serum IgE titres were induced in primed animals in a dose-independent way. In contrast, intermediate and low responders differed in the onset of the production of Cooperia-specific serum IgG1. Furthermore, not only the onset but also the level of total serum IgE significantly differed between intermediate and low responders. Phenotypic and functional analysis of B lymphocytes revealed that (i) priming induced the generation of memory B cells which upon challenge readily differentiated into antibody secreting cells; (ii) sensitised B cells were more efficiently recruited to the intestinal effector sites; (iii) based on the expression of CD62L and CD86 two distinct B cell subpopulation could be differentiated. CD62L(+)CD86(-) B cells that were likely lymphocytes not yet activated and with an enhanced recirculation capacity, and CD62L(-)CD86(+) B cells that were activated B cells with a reduced recirculation ability; and finally (iv) the increased expression of CD86 and subsequent correlations with parameters of the T helper 2 immune response induced by C. oncophora, suggested that CD86- interactions are involved in the generation of protective immunity against Cooperia. (C) 2003 Australian Society for Parasitology Inc. Published by Elsevier Ltd. All rights reserved.

    Research areas

  • DAIRY REPLACEMENT STOCK, SERUM IGE RESPONSES, T-CELLS, GASTROINTESTINAL NEMATODES, bovine, TRICHOSTRONGYLUS-COLUBRIFORMIS, OSTERTAGIA-OSTERTAGI, B cell, host responder type, IMMUNE-RESPONSE, CD86, LYMPHOID-TISSUES, mucosal immunity, MONOCLONAL-ANTIBODIES, HAEMONCHUS-CONTORTUS INFECTION, gastro-intestinal nematode

ID: 7555325