Progression from insulitis to beta-cell destruction in NOD mouse requires L3T4+ T-lymphocytes.

Abstract:

:The identity of the cells responsible for beta-cell destruction in type I (insulin-dependent) diabetes is still uncertain. L3T4+ T-lymphocytes have a role in the initiation of insulitis and in damaging transplanted allogeneic islets in nonobese diabetic (NOD) mice. The role of L3T4+ T-lymphocytes in destruction of beta-cells of the NOD mouse was studied in cyclophosphamide (CY)-induced diabetic NOD mice with a rat anti-L3T4 monoclonal antibody (MoAb). After administration of CY, most untreated animals became diabetic, whereas all antibody-treated animals remained normoglycemic. Insulitis was still present in MoAb-treated animals, but immunocytochemical staining showed rat antibody blocking the L3T4 antigen on T-lymphocytes. This study provides further evidence that L3T4+ T-lymphocytes are critical to the process of beta-cell destruction in NOD mice. The means by which L3T4+ cells exert their effect remains to be clarified.

journal_name

Diabetes

journal_title

Diabetes

authors

Charlton B,Mandel TE

doi

10.2337/diab.37.8.1108

subject

Has Abstract

pub_date

1988-08-01 00:00:00

pages

1108-12

issue

8

eissn

0012-1797

issn

1939-327X

journal_volume

37

pub_type

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