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M9640681.TXT
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1996-03-04
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Document 0681
DOCN M9640681
TI CD8 T cell clones from young nonobese diabetic (NOD) islets can transfer
rapid onset of diabetes in NOD mice in the absence of CD4 cells.
DT 9604
AU Wong FS; Visintin I; Wen L; Flavell RA; Janeway CA Jr; Section of
Immunobiology, Yale University School of Medicine, New; Haven,
Connecticut 06510, USA.
SO J Exp Med. 1996 Jan 1;183(1):67-76. Unique Identifier : AIDSLINE
MED/96136749
AB T cells play an important role in the pathogenesis of diabetes in the
nonobese diabetic (NOD) mouse. CD8 cytotoxic T cell lines and clones
were generated from the lymphocytic infiltrate in the islets of
Langerhans of young (7-wk-old). NOD mice by growing them on (NOD x
B6-RIP-B7-1)F1 islets. These cells proliferate specifically to NOD
islets and kill NOD islets in vitro. The cells are restricted by H-2Kd,
and all bear T cell antigen receptor encoded by V beta 6. When these CD8
T cell lines and clones are adoptively transferred to irradiated female
NOD, young NOD-SCID, and CB17-SCID mice, diabetes occurs very rapidly,
within 10 d of transfer and without CD4 T cells.
DE Amino Acid Sequence Animal Antigens, CD80/GENETICS/*IMMUNOLOGY Base
Sequence Clone Cells Cytokines/BIOSYNTHESIS CD4-Positive
T-Lymphocytes/*IMMUNOLOGY CD8-Positive T-Lymphocytes/*IMMUNOLOGY
Diabetes Mellitus, Non-Insulin-Dependent/*IMMUNOLOGY Female
Immunohistochemistry Immunotherapy, Adoptive Insulin/GENETICS Islets
of Langerhans/*IMMUNOLOGY Lymphocyte Transformation Membrane
Glycoproteins/BIOSYNTHESIS Mice Mice, Inbred BALB C Mice, Inbred
C57BL Mice, Inbred NOD Mice, SCID Molecular Sequence Data
Pancreas/ANATOMY & HISTOLOGY Promoter Regions (Genetics)/GENETICS
Support, Non-U.S. Gov't Support, U.S. Gov't, P.H.S. JOURNAL ARTICLE
SOURCE: National Library of Medicine. NOTICE: This material may be
protected by Copyright Law (Title 17, U.S.Code).