The gamma class chemokine Lymphotactin regulates T cell trafficking from blood to lymph nodes and is instrumental in recruiting cells to the mucosa. We are studying the structure and function of Lymphotactin to increase our comprehension of its biological functions and to devise rational design strategies to produce new drugs based on this molecule. Abstract We cloned cDNA for the rhesus and human Lymphotactin genes. The cDNA clones were expressed in E. coli and recombinant proteins were purified. The recombinant Lymphotactin was fully active in biological assays and we noted a species specificity wherein the rhesus molecule was at least five-times more active on rhesus cells than on human cells. A similar specificity was observed for human Lymphotactin. We have produced sufficient Lymphotactin and 15N-Lymphotactin for structural analysis by NMR and this effort is underway. In addition we have generated chimeric SHIV that express Lymphotactin in place of the nef gene. These viruses are stable during in vitro passages and we are preparing stocks for animal infection studies. FUTURE DIRECTIONS We are developing recombinant SHIV that express lymphotactin and these viruses will be tested for mucosal transmission efficiency. Additionally, we are developing assays for lymphotactin expression in vivo and for understanding the role of this chemokine in mucosal virus transmission and mucosal vaccine efficacy. KEY WORDS AIDS, chemokine, structure, lymphocyte, trafficking, vaccine

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Primate Research Center Grants (P51)
Project #
5P51RR000167-38
Application #
6277663
Study Section
Project Start
1998-05-01
Project End
1999-04-30
Budget Start
1997-10-01
Budget End
1998-09-30
Support Year
38
Fiscal Year
1998
Total Cost
Indirect Cost
Name
University of Wisconsin Madison
Department
Type
DUNS #
161202122
City
Madison
State
WI
Country
United States
Zip Code
53715
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