Lactobacilli-expressed single-chain variable fragment (scFv) specific for intercellular adhesion molecule 1 (ICAM-1) blocks cell-associated HIV-1 transmission across a cervical epithelial monolayer

被引:41
作者
Chancey, Caren J.
Khanna, Kristen V.
Seegers, Jos F. M. L.
Zhang, Guang Wen
Hildreth, James
Langan, Abigail
Markham, Richard B.
机构
[1] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Mol Microbiol & Immunol, Baltimore, MD 21205 USA
[2] Erasmus Univ, Rotterdam, Netherlands
[3] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Pharmacol & Mol Sci, Baltimore, MD 21205 USA
[4] Meharry Med Coll, Nashville, TN 37208 USA
关键词
D O I
10.4049/jimmunol.176.9.5627
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The vaginal and cervical epithelia provide an initial barrier to sexually acquired HIV-1 infection in women. To study the interactions between HIV-1-infected cells or cell-free HIV-1 and the reproductive epithelium, the transmission of HIV-1 by infected cells or cell-free virus across human cervical epithelial cells was examined using a Transwell culture system. Cell-associated HIV-1 was transmitted more efficiently than cell-free virus, and monocyte-associated virus was transmitted most efficiently. Abs to ICAM-1 added to the apical side of the epithelium blocked cell-mediated transepithelial HIV-1 transmission in vitro. When used in a previously described model of vaginal HIV-1 transmission in human PBL-SCID mice, anti-murine ICAM-1 Abs (0.4 mu g/10 mu l) also blocked vaginal transmission of cell-associated HIV-1 in vivo. To evaluate a candidate delivery system for the use of this Ab as an anti-HIV-1 microbicide, anti-ICAM single-chain variable fragment Abs secreted by transformed lactobacilli were evaluated for their protective efficacy in the Transwell model. Like the intact Ab and Fab derived from it, the single-chain variable fragment at a concentration of 6.7 mu g/100 mu l was able to reduce HIV-1 transmission by 70 +/- 5 %. These data support the potential efficacy of an anti-ICAM Ab delivered by lactobacilli for use as an anti-HIV-1 microbicide.
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页码:5627 / 5636
页数:10
相关论文
共 62 条
[1]   Cytomechanics of cadherin-mediated cell-cell adhesion [J].
Adams, CL ;
Nelson, WJ .
CURRENT OPINION IN CELL BIOLOGY, 1998, 10 (05) :572-577
[2]   Mechanisms of epithelial cell-cell adhesion and cell compaction revealed by high-resolution tracking of E-cadherin-green fluorescent protein [J].
Adams, CL ;
Chen, YT ;
Smith, SJ ;
Nelson, WJ .
JOURNAL OF CELL BIOLOGY, 1998, 142 (04) :1105-1119
[3]  
ANDERSON DJ, 1983, NEW ENGL J MED, V309, P984
[4]  
Anderson E.W., 1998, J SERVICE RES, V1, P5, DOI DOI 10.1177/109467059800100102
[5]   CCR5- and CXCR4-utilizing strains of human immunodeficiency virus type 1 exhibit differential tropism and pathogenesis in vivo [J].
Berkowitz, RD ;
Alexander, S ;
Bare, C ;
Linquist-Stepps, V ;
Bogan, M ;
Moreno, ME ;
Gibson, L ;
Wieder, ED ;
Kosek, J ;
Stoddart, CA ;
McCune, JM .
JOURNAL OF VIROLOGY, 1998, 72 (12) :10108-10117
[6]   Transcytosis of infectious human immunodeficiency virus across a tight human epithelial cell line barrier [J].
Bomsel, M .
NATURE MEDICINE, 1997, 3 (01) :42-47
[7]   A SEVERE COMBINED IMMUNODEFICIENCY MUTATION IN THE MOUSE [J].
BOSMA, GC ;
CUSTER, RP ;
BOSMA, MJ .
NATURE, 1983, 301 (5900) :527-530
[8]   Presence of host ICAM-1 in laboratory and clinical strains of human immunodeficiency virus type 1 increases virus infectivity and CD4+-T-cell depletion in human lymphoid tissue, a major site of replication in vivo [J].
Bounou, S ;
Leclerc, JE ;
Tremblay, MJ .
JOURNAL OF VIROLOGY, 2002, 76 (03) :1004-1014
[9]   Mucosal transmission of cell-associated and cell-free feline immunodeficiency virus [J].
Burkhard, MJ ;
Obert, LA ;
ONeil, LL ;
Diehl, LJ ;
Hoover, EA .
AIDS RESEARCH AND HUMAN RETROVIRUSES, 1997, 13 (04) :347-355
[10]   Expression of a candidate cadherin in T lymphocytes [J].
Cepek, KL ;
Rimm, DL ;
Brenner, MB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (13) :6567-6571