Peripheral T cell activation and deletion induced by transfer of lymphocyte subsets expressing endogenous or exogenous mouse mammary tumor virus

Autor: Gary A. Waanders, Werner Held, A N Shakhov, H R MacDonald, Hans Acha-Orbea, O Karapetian
Jazyk: angličtina
Rok vydání: 1993
Předmět:
Male
Adoptive cell transfer
Receptors
Antigen
T-Cell
alpha-beta

Lymphocyte
T cell
Immunology
Lymphocyte Activation
Minor Lymphocyte Stimulatory Antigens
Mice
Mammary Glands
Animal

Proviruses
T-Lymphocyte Subsets
parasitic diseases
medicine
Animals
Immunology and Allergy
Cytotoxic T cell
Mice
Inbred BALB C

Antigens
CD4/biosynthesis

Female
Mammary Glands
Animal/microbiology

Mammary Tumor Virus
Mouse/genetics

Mammary Tumor Virus
Mouse/immunology

Mice
Inbred CBA

Minor Lymphocyte Stimulatory Antigens/biosynthesis
Proviruses/genetics
Proviruses/immunology
Receptors
Antigen
T-Cell
alpha-beta/biosynthesis

T-Lymphocyte Subsets/immunology
T-Lymphocyte Subsets/microbiology
Tumor Virus Infections/immunology
biology
Mouse mammary tumor virus
Articles
T lymphocyte
biology.organism_classification
Virology
Molecular biology
Tumor Virus Infections
medicine.anatomical_structure
Mammary Tumor Virus
Mouse

CD4 Antigens
CD8
Zdroj: Journal of Experimental Medicine, vol. 177, no. 5, pp. 1359-1366
The Journal of Experimental Medicine
Popis: Murine T cell reactivity with products of the minor lymphocyte stimulatory (Mls) locus correlates with the expression of particular variable (V) domains of the T cell receptor (TCR) beta chain. It was recently demonstrated that Mls antigens are encoded by an open reading frame (ORF) in the 3' long terminal repeat of either endogenous or exogenous mouse mammary tumor virus (MMTV). Immature thymocytes expressing reactive TCR-V beta domains are clonally deleted upon exposure to endogenous Mtv's. Mature T cells proliferate vigorously in response to Mls-1a (Mtv-7) in vivo, but induction of specific anergy and deletion after exposure to Mtv-7-expressing cells in the periphery has also been described. We show here that B cells and CD8+ (but not CD4+) T cells from Mtv-7+ mice efficiently induce peripheral deletion of reactive T cells upon transfer to Mtv-7- recipients, whereas only B cells stimulate specific T cell proliferation in vivo. In contrast to endogenous Mtv-7, transfer of B, CD4+, or CD8+ lymphocyte subsets from mice maternally infected with MMTV(SW), an infectious homologue of Mtv-7, results in specific T cell deletion in the absence of a detectable proliferative response. Finally, we show by secondary transfers of infected cells that exogenous MMTV(SW) is transmitted multidirectionally between lymphocyte subsets and ultimately to the mammary gland. Collectively our data demonstrate heterogeneity in the expression and/or presentation of endogenous and exogenous MMTV ORF by lymphocyte subsets and emphasize the low threshold required for induction of peripheral T cell deletion by these gene products.
Databáze: OpenAIRE