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Journal ArticleDOI

Evidence that the thy-1 molecule is the target for t cell mitogenic antibody against brain-associated antigens.

Barry Jones
- 01 Jan 1983 - 
- Vol. 13, Iss: 8, pp 678-684
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TLDR
The coordinated genetic control of the surface levels of the Thy‐1 determinant and the mitogenic determinant suggests that both determinants are situated on the same molecule in the T cell membrane.
Abstract
Rabbit anti-mouse brain (RaMBr) antiserum can induce Lyt-1+, Lyt-2-, T cells to proliferate and stimulates the same T cell subset to induce B cell proliferation. The aim of this report is to demonstrate that the mitogenic determinant recognized on the T cell surface by RaMBr antiserum is located on the Thy-1 molecule expressing the products of the Thy-1a and Thy-1b alleles. Evidence is drawn from serological and genetic experiments. The brain T cell cross-reactive, mitogenic determinant is not expressed on Thy-1- mutants of the BW5147 T cell lymphoma that fail to express the Thy-1 molecule but do express other T cell surface proteins such as T-200 and gp 69, 71. Monoclonal anti-Thy-1.1 and anti-Thy-1.2 antibodies block the binding to the appropriate T cells of the majority of the serum antibody from RaMBr antiserum. The absorption of mitogenic antibody was blocked in a similar fashion, thus demonstrating the close association of the determinant and the Thy-1 antigen defined by monoclonal alloantibodies. The mitogenic and Thy-1.1 determinants are probably located on the same molecule because of the data obtained with the BW5147 Thy-1- mutants and the observation that Thy-1a T cells, which express a lower level of surface Thy-1 than Thy-1b T cells, also express lower levels of the determinant recognized by RaMBr antiserum. Furthermore, in (AKR x DBA/2)F1 mice (Thy-1a/b) which express less Thy-1.1 antigen than Thy-1.2 at the surface, the mitogenic determinant was found to be preferentially associated with Thy-1.2. The coordinated genetic control of the surface levels of the Thy-1 determinant and the mitogenic determinant suggests that both determinants are situated on the same molecule in the T cell membrane.

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Citations
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Both a monoclonal antibody and antisera specific for determinants unique to individual cloned helper T cell lines can substitute for antigen and antigen-presenting cells in the activation of T cells.

TL;DR: The specificity of these antibodies and their ability to stimulate cloned helper T cells in the absence of antigen and antigen-presenting cells strongly suggest that these antibodies are directed against antigen and/or Ia recognition sites on the T cell.
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Induction of Airway Mucus Production By T Helper 2 (Th2) Cells: A Critical Role For Interleukin 4 In Cell Recruitment But Not Mucus Production

TL;DR: It is suggested that IL-4 is crucial for Th2 cell recruitment to the lung and for induction of inflammation, but has no direct role in mucus production.
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The relationship of IL-4- and IFNγ-producing T cells studied by lineage ablation of IL-4-producing cells

TL;DR: Results show that effector cells producing either IL-4 or IFN gamma have a common precursor, which expresses the IL-3 gene, and this results show that naive T cells and effector Th1- and Th2-type cells are separated by lineage.
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T Helper 1 Cells and Interferon γ Regulate Allergic Airway Inflammation and Mucus Production

TL;DR: New regulatory pathways for mucus production are identified; mucus can be induced by Th2 and non-Th2 inflammatory responses in the lung, both of which are inhibited by IFN-γ.
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Th2-induced airway mucus production is dependent on IL-4Ralpha, but not on eosinophils.

TL;DR: These studies show definitively that IL-5, eosinophils, or mast cells are not essential, but signaling through IL-4Ralpha is critically important in Th2 cell stimulation of mucus production.
References
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Journal Article

Properties and Applications of Monoclonal Antibodies Directed against Determinants of the Thy-1 Locus

TL;DR: Treatment of peripheral lymphocyte populations with monoclonal antibody plus C eliminated effector cytotoxic T lymphocytes, their precursors, and the mitogenic response to Con A, but did not affect the response to LPS.
Journal ArticleDOI

Immune responses in vitro. I. Culture conditions for antibody synthesis.

TL;DR: The addition of mercaptoethanol to the culture medium and the optimization of other components has substantially improved the response of mouse spleen cells to in vitro immunization with heterologous RBC and may facilitate the study of the genetic control of antibody synthesis.
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Complete amino acid sequence of an HLA-DR antigen-like beta chain as predicted from the nucleotide sequence: similarities with immunoglobulins and HLA-A, -B, and -C antigens.

TL;DR: The complete nucleotide sequence of an HLA-DR antigen-like beta-chain cDNA clone was determined and data establish that the major histocompatibility antigens of class I and class II type and the constant regions of immunoglobulin are evolutionarily related.
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Cooperative interaction of B lymphocytes with antigen-specific helper T lymphocytes is MHC restricted.

TL;DR: It is concluded that the antigen-specific cooperative interactions between Th and B cells are themselves MHC restricted, and that B cells bearing the wrong MHC-encoded antigens cannot be activated by addition of APCs matched to the Th cell but differing from the B cell at MHC.
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Production and characterization of cytotoxic Thy-1 antibody-secreting hybrid cell lines. Detection of T cell subsets.

TL;DR: Responses to Thy‐1 were used as a model system to examine parameters which affect the production of antibody‐secreting lines derived from somatic cell hybridization, and variables in the choice and dose of antigen, the response kinetics and in the fusion procedures were optimized.
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