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Updated: Jun 20, 2026

Application of Long-term cultured Interferon-γ Enzyme-linked Immunospot Assay for Assessing Effector and Memory T Cell Responses in Cattle
Published on: July 11, 2015
CD62L defines a subset of pathogen-specific bovine CD4 with central memory cell characteristics
Philippe Totté1, Christophe Duperray, Laurence Dedieu
1CIRAD, UMR1304 Control of Exotic and Emerging Animal Diseases, Montpellier, France. philippe.totte@cirad.fr
Insights
Central memory T cells (Tcm) were identified in cattle, offering insights into ruminant immunity. CD62L can serve as a marker for Tcm in cattle infections and vaccine development.
Area of Science:
- Veterinary Immunology
- Ruminant immunology
- T cell subsets
Background:
- Central memory T cells (Tcm) are crucial for long-term immunity but uncharacterized in cattle.
- Pathogen-specific memory CD4(+) T cells are key to understanding adaptive immunity in ruminants.
Purpose of the Study:
- To characterize central memory T cells (Tcm) in cattle.
- To identify markers for Tcm in ruminant immune responses.
Main Methods:
- Phenotypic and functional analysis of CD4(+) T cells in cattle post-Mycoplasma mycoides subsp. mycoides small colony (MmmSC) infection.
- Cell sorting and transcript analysis (CCR7, CCR5) of T cell subsets.
- Recall stimulation assays to assess T cell proliferation and cytokine production (IFN-gamma).
Main Results:
- Two distinct pathogen-specific memory CD4(+) T cell subsets were identified: CD45RO(+)CD45R(-)CD62L(-) and CD45RO(+)CD45R(-)CD62L(+).
- The CD62L(-) subset was associated with high IFN-gamma production, while the CD62L(+) subset showed higher proliferation.
- CD62L(+) T cells exhibited characteristics of Tcm, including CD62L and CCR7 expression, suggesting lymph node homing capabilities.
Conclusions:
- This study demonstrates the existence of central memory T cells (Tcm) in cattle.
- CD62L can be utilized as a marker for monitoring Tcm in ruminant infections and vaccine development.
Abstract:
Central memory T cells (Tcm) have not previously been characterized in cattle and any other ruminant species. Here we described two phenotypically and functionally different subsets of pathogen-specific memory CD4(+) T cells in cattle that survived infection with Mycoplasma mycoides subsp. mycoides small colony (MmmSC). The first subset is CD45RO(+)CD45R(-)CD62L(-) and comprises two thirds of IFN-gamma producing CD4(+) T cells after MmmSC recall stimulation. The second is CD45RO(+)CD45R(-)CD62L(+) and represents the majority of proliferating CD4(+) T cells after 7 days of stimulation. Cell sorting experiments confirmed that both CD4(+)CD62L(+) and CD4(+)CD62L(-) subsets are present in vivo and proliferate independently in recall responses to MmmSC. In addition, MmmSC stimulation strongly decreased CCR7 and increased CCR5 transcripts levels in CD4(+)CD62L(-) cells whereas CD4(+)CD62L(+) were only slightly affected. High levels of recall proliferation but low IFN-gamma production, together with the capacity to preferentially migrate through the lymph nodes (i.e., expression of CD62L and CCR7), are characteristics of Tcm, in humans and mice. Tcm are associated with long-term protective immunity and a privileged target for vaccine development. Our results demonstrate the existence of Tcm in cattle and suggest that CD62L may serve as a marker to monitor Tcm in infections and vaccine development studies in ruminant.
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