• No results found

Human Immunodeficiency Virus Persistence and Production in T-Cell Development

N/A
N/A
Protected

Academic year: 2020

Share "Human Immunodeficiency Virus Persistence and Production in T-Cell Development"

Copied!
9
0
0

Loading.... (view fulltext now)

Full text

Loading

Figure

FIG. 1. Thymocyte development scheme. (A) Combinations of an-tibodies were used to identify thymocytes at five distinct stages of
FIG. 2. X4 HIV-1 replicates in immature thymocytes, while R5 HIV-1 replicates in mature thymocytes in HIV-1-infected SCID-hu mice.Thymocytes were obtained from HIV-1-infected implants in SCID-hu mice at 19 days (NL4-3) and 26 days (JR-CSF) postinfection
FIG. 3. R5 and X4 HIV-1 proviral burdens in thymocyte subsets atdifferent stages of maturation
FIG. 4. HIV-1 coreceptor expression in thymocytes at five devel-opmental stages. CCR5 and CXCR4 expression at stages I-P to IV of
+2

References

Related documents

BRONCHIAL ASTHMA IN CHILDREN & ASSESSMENT OF SEVERITY OF ASTHMA AND ITS CORRELATION WITH SERUM IgE

Because of the general relatedness of lentiviruses, it is con- ceivable that additional lentivirus genes are also required for HIV replication but exist in a surrogate or

Direct Immunofluorescence study: Linear deposition of IgA along the basement membrane zone is seen. There may also

CVB3 infection of female mice results in preferential Th2 cell responses, but in vivo treatment of fe- males with androgens can shift the dominant CD4 1 T-cell response toward the

the N protein in neurons infected with CVS-B2c and CVS-N2c differed (Fig. 2) despite the identical amino acid sequences of this protein in the variants (16), the differences in

HTLV-1 envelope-dependent entry, we examined the inhibi- tory effect of mature gp46 and gp21 proteins, which were purified from an HTLV-1-infected cell line (12, 26), on syncy-

Accumulation of mutant virus in organs of infected turnip deter- mined by dot blot analysis of total viral DNA isolated from tissues at 26 days postinfection of plants infected

Given the rarity of naturally occurring mutations which result in enhanced initiation of translation and previous evi- dence that domain 3 is essential for IRES activity of FMDV