A novel monoclonal antibody specific for canine CD25 (P4A10): selection and evaluation of canine Tregs.

Publication Type:

Journal Article

Source:

Veterinary immunology and immunopathology, Volume 135, Issue 3-4, p.257-65 (2010)

Keywords:

2010, Animals, Antibodies, Monoclonal, Antibody Development Core Facility, Antibody Specificity, Base Sequence, Binding, Competitive, Biologics Production Core Facility, Blotting, Western, Center-Authored Paper, Clinical Research Division, Comparative Medicine Core Facility, DNA Primers, Dogs, Female, Flow Cytometry Core Facility, Forkhead Transcription Factors, Humans, Immunoglobulin G, Interleukin-2 Receptor alpha Subunit, Lymphocyte Activation, Male, Shared Resources, T-Lymphocytes, Regulatory

Abstract:

A monoclonal antibody (mAb), P4A10, was made to the canine interleukin-2 receptor alpha chain (IL-2Ralpha; p55; Tac antigen; CD25) to facilitate studies of canine regulatory T-cells (Treg). By non-reduced Western blot, P4A10 bound to a 55kDa protein, the size of human IL-2Ralpha. In flow cytometry assays, it reacted with a minor population of circulating dog CD3(+)CD4(+) T-cells and the majority (>60%) of in vitro PMA-Ionomycin (PMA-IO)-activated canine CD3(+) T-cells. P4A10 recognized a hematopoietic cell population enriched for FoxP3+ cells as measured by flow cytometry. The P4A10-selected fractions of T-cells had significantly increased copy numbers of CD25, FoxP3, IL-10, and TGFbeta as detected by RT-PCR (reverse transcriptase-PCR) compared to the negative fractions. The P4A10-selected cells inhibited (3)H (tritiated) thymidine incorporation in a mixed leukocyte reaction (MLR) containing responders of the same origin. P4A10-selected T-cells from fresh peripheral blood mononuclear cells had less FoxP3 (p=0.07) by qRT-PCR (quantitative RT-PCR) and were less suppressive (p=0.01) than in vitro alloantigen-activated Treg. The mAb P4A10 is specific for canine CD25 and can be used to facilitate studies of CD25+FoxP3+ Treg in this clinically relevant large animal model.