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PMID: 9665085 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Interferon-gamma receptor signaling is not required in the effector phase of the alloimmune response.

Transplantation ·Vol. 65 ·No. 12 ·1998-06-27 ·Pages 1649-52

Steiger JU, Nickerson PW, Hermle M, Thiel G, Heim MH

Abstract

Gene transcripts for the Thl cytokines interleukin (IL)-2 and interferon-gamma (IFN-gamma) are frequently detected during allograft rejection. The relative importance of these cytokines in facilitating allograft rejection is unclear. Recently, we have shown that IL-2-deficient mice reject islet allografts. In the IL-2-deficient system, IFN-gamma gene transcripts are abundantly expressed. To determine the relative importance of IFN-gamma-dependent effector mechanisms in mediating allograft rejection, the present study utilized IFN-gamma receptor-deficient mice as islet allograft recipients. Grafts were analyzed by immunohistology, and cytokine expression was measured by competitive template reverse transcriptase polymerase chain reaction. IFN-gamma receptor-deficient mice reject islet allografts by a process that is T cell-dependent. Although IFN-gamma receptor signaling is absent, these mice do not show a clear Th2 type response. Although the signals evoked through the IFN-gamma receptor may play a role, they are not essential to allograft rejection.

MeSH Terms
Animals Graft Rejection Interferon-gamma/genetics Interleukin-2/genetics Mice Mice, Inbred C57BL Mice, Knockout Receptors, Interferon/genetics,physiology Transplantation, Homologous/immunology
Chemicals
Interleukin-2 Receptors, Interferon interferon gamma receptor Interferon-gamma
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Steiger J U
Department of Research, University Hospital Basel, Switzerland. [email protected]
Nickerson P W
Hermle M
Thiel G
Heim M H
Article Info
Journal
Transplantation
Abbr.
Transplantation
ISSN
0041-1337
Published
1998-06-27
Pages
1649-52
Language
English
Region
United States
NLM ID
0132144
Subset
IM
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