|
|
||||||||
From the Arthritis and Rheumatism Branch, National Institute of Arthritis, Metabolism and Digestive Diseases and Clinical Immunology Section, Laboratory of Microbiology and Immunology Branch, National Institute of Dental Research, National Institutes of Health, Bethesda, Maryland 20014
Abstract
Natural thymocytotoxic antibody (NTA) which occurs in high titer in New Zealand Black (NZB) mice was compared with AKR anti-
(C3H) antiserum for ability to induce redistribution of C57BL/6 thymocyte surface antigen. NTA reacted with both thymocytes and brain cells bearing either the
-AKR or
-C3H alloantigens and was found to be an IgM antibody. Anti-
(C3H) was purified to obtain the IgG fraction which was used in these studies. Neither NTA nor anti-
antibody induced cap formation alone, however, both formed caps upon the addition of specific anti-immunoglobulin sera. Studies involving the sequential exposure of thymocytes to both antibodies demonstrated that
and NTA reactive antigen co-migrate on the thymocyte surface. These studies suggest that NTA reacts with a determinant common to both the
-AKR and
-C3H alloantigens.
Footnotes
1 Present address: Children's Cancer Research Foundation, 35 Binney Street, Boston, Massachusetts.
2 Reprint request should be sent to A. D. Steinberg, M.D., Building 10, Room 8D-19, National Institutes of Health, Bethesda, Md. 20014.
This article has been cited by other articles:
![]() |
M. Gui, D. L. Wiest, J. Li, D. Kappes, R. R. Hardy, and K. Hayakawa Peripheral CD4+ T Cell Maturation Recognized by Increased Expression of Thy-1/CD90 Bearing the 6C10 Carbohydrate Epitope J. Immunol., November 1, 1999; 163(9): 4796 - 4804. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Krakauer, W Strober, D. Rippeon, and T. Waldmann Prevention of autoimmunity in experimental lupus erythematosus by soluble immune response suppressor Science, April 1, 1977; 196(4285): 56 - 59. [Abstract] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |