Cloning, sequencing, expression and characterization of the feline CD28 / CD80 accessory signaling complex /

T cell activation is mediated through two distinct signaling

Bibliographic Details
Main Author: Hash, Stephen Martin
Format: Thesis Book
Language:English
Published: [Place of publication not identified] : [publisher not identified] ; 1997.
Subjects:
Online Access:http://proxy.library.tamu.edu/login?url=http://proquest.umi.com/pqdweb?did=739887471&sid=1&Fmt=2&clientId=2945&RQT=309&VName=PQD
Description
Summary:T cell activation is mediated through two distinct signaling
events. In human and murine systems, it has been
demonstrated that an antigen specific interaction mediated
through recognition by the T cell receptor of antigen
presented in the context of MHC delivers the primary signal,
while the secondary signal is delivered by an antigen
independent interaction (Allison and Lanier, 1987). The
interaction between CD28 on the T cell and CD80 (B7-1) on the
antigen presenting cell has been established as an essential
element in the delivery of this secondary signal (Linsley et
al., 1993). In rodents and primates, signals delivered
through the cross-linking of CD28 by CD80 in conjunction with
TCR mediated signaling leads to augmented T cell
proliferation and cytokine production, while in the absence
of the signal, TCR cross linking results in clonal anergy
(Schwartz, 1992). Despite the importance of the CD28/CD80
interaction in the development of the immune response, these
molecules have only been isolated from a limited number of
species. CD28 has been cloned in rodent and primate species
as well as the rabbit, with a seemingly analogous receptor
obtained in the chicken. Conversely, CD80 has only been
cloned in rodent and primate species. The feline system is
evolutionarily divergent from primates and rodents. Due to
the importance of the binding of CD28 and CD80 in the
development and maintainence of a functional T cell response,
these accessory molecules were cloned, their sequence
determined and expressed to confirm the interaction. The
isolation of these molecules will provide valuable markers
for and mediators of the feline T cell response and might
potentially establish an evolutionary intermediate to which
previously cloned molecules might be compared. Further, the
feline system is increasingly important as a potential model
of human disease, specifically HIV, and a more complete
understanding of the pathogenicity of retroviral infections
in the cat may lead to answers about analogous diseases in
other systems. The more readily that the immune system is
characterized in the feline may increase the ease with which
infections are understood in that system as well as others.
Item Description:Vita.
"Major Subject: Veterinary Microbiology".
In title, numerals are used.
Physical Description:xvii, 168 leaves : illustrations ; 28 cm.
Issued also on microfiche from University Microfilms Inc.
Bibliography:Includes bibliographical references: pages 141-167.