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Journal of Virology, July 2000, p. 6386-6393, Vol. 74, No. 14
Institute of Medical Microbiology, Immunology
and Hygiene, Technical University of Munich, 81675 Munich,1 and Paul Ehrlich Institute,
63225 Langen,2 Germany
Received 5 January 2000/Accepted 26 April 2000
Mice harbor a family of endogenous retroviruses, the mouse mammary
tumor viruses (MMTV), which encode superantigens. These superantigens
are responsible for the deletion of T cells expressing certain V
0022-538X/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Functional Analysis of the env Open
Reading Frame in Human Endogenous Retrovirus
IDDMK1,222 Encoding Superantigen Activity
chains of the T-cell receptor in the thymus. Human T cells are able to
recognize MMTV-encoded superantigens presented by human major
histocompatibility complex class II-positive cells. Owing to this and
to the similarity of the human and murine immune systems, it was
speculated that human endogenous retroviruses might also code for
superantigens. Recently, it was reported that a proviral clone
(IDDMK1,222) of the human endogenous retrovirus family
HTDV/HERV-K encodes a superantigen. The putative superantigen gene was
located within the env region of the virus. Stimulated by
these findings, we amplified by PCR and cloned into eucaryotic expression vectors open reading frames (ORFs) which were identical or
very similar to IDDMK1,222. When we transfected these
vectors into A20 cells, a murine B-cell lymphoma, we were able to
demonstrate mRNA expression and protein production. However, we did not
find any evidence that the ORF stimulated human or murine T cells in a
V
-specific fashion, the most prominent feature of superantigens.
*
Corresponding author. Mailing address: Institute of
Medical Microbiology, Immunology and Hygiene, Technical University of Munich, Trogerstr. 9, 81675 Munich, Germany. Phone: 49/89/4140-4187. Fax: 49/89/4140-4868. E-mail:
Thomas.Miethke{at}lrz.tu-muenchen.de.
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