T Helper 1 (Th1) and Th2 Characteristics Start to Develop During T Cell Priming and Are Associated with an Immediate Ability to Induce Immunoglobulin Class Switching

Author:

Toellner Kai-Michael1,Luther Sanjiv A.11,Sze Daniel M.-Y.1,Choy Richard K.-W.1,Taylor Dale R.1,MacLennan Ian C.M.1,Acha-Orbea Hans11

Affiliation:

1. From the Department of Immunology, University of Birmingham Medical School, Birmingham B15 2TT United Kingdom; the Ludwig Institute for Cancer Research, Lausanne Branch; and the Institute of Biochemistry, University of Lausanne, 1066 Epalinges, Switzerland

Abstract

The respective production of specific immunoglobulin (Ig)G2a or IgG1 within 5 d of primary immunization with Swiss type mouse mammary tumor virus [MMTV(SW)] or haptenated protein provides a model for the development of T helper 1 (Th1) and Th2 responses. The antibody-producing cells arise from cognate T cell B cell interaction, revealed by the respective induction of Cγ2a and Cγ1 switch transcript production, on the third day after immunization. T cell proliferation and upregulation of mRNA for interferon γ in response to MMTV(SW) and interleukin 4 in response to haptenated protein also starts during this day. It follows that there is minimal delay in these responses between T cell priming and the onset of cognate interaction between T and B cells leading to class switching and exponential growth. The Th1 or Th2 profile is at least partially established at the time of the first cognate T cell interaction with B cells in the T zone. The addition of killed Bordetella pertussis to the hapten–protein induces nonhapten-specific IgG2a and IgG1 plasma cells, whereas the anti-hapten response continues to be IgG1 dominated. This indicates that a Th2 response to hapten–protein can proceed in a node where there is substantial Th1 activity.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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