TY - JOUR
T1 - Increased CCR5 and CXCR4 expression in Ethiopians living in Israel
T2 - Environmental and constitutive factors
AU - Kalinkovich, Alexander
AU - Borkow, Gadi
AU - Weisman, Ziva
AU - Tsimanis, Alexander
AU - Stein, Miguel
AU - Bentwich, Zvi
N1 - Funding Information:
We thank Dr Janis V. Giorgi for providing the “Protocol for Estimating the Number of CD38 Molecules on the CD8+ T Lymphocytes of HIV-Infected Individuals” and Dr Alan L. Landay for helpful suggestions and the gift of reagents used in this study. This work was supported in part by grants from The Institute of Advanced Therapy, Center of Excellence in AIDS Research in Israel and the Horowitz Foundation. A. Kalinkovich is a KAMEA fellow.
PY - 2001
Y1 - 2001
N2 - HIV coreceptors play a major role in determining susceptibility and HIV cell tropism. The present work studied whether the high expression of these coreceptors found on lymphocytes and monocytes of Ethiopian immigrants to Israel (ETH) is the result of environmental and/or constitutive genetic factors. The study of 26 ETH shortly after their arrival to Israel (new ETH), 22 ETH in Israel over 7 years (old ETH), and 20 Caucasian Israelis (non-ETH) enabled us to address this issue. The new ETH had elevated levels of activated HLA-DR+CD4+ and CD38+CD8+ cells in comparison with both old ETH and non-ETH groups (P < 0.01), most probably related to chronic helminthic infections. Surface CCR5 expression, i.e., the percentage of CCR5+ cells and the number of CCR5 molecules/cell, was higher (2- to 3- and 8- to 31-fold, respectively) in activated than in nonactivated CD4+ cells, in all groups. However, CCR5 expression, in both activated and nonactivated CD4+ cells, was higher in both ETH groups than in the non-ETH group. CXCR4 expression was higher in nonactivated CD4+ cells in all groups and was also higher in both ETH groups, in both activated and nonactivated CD4+ cells, than in the non-ETH group. These findings suggest that constitutive factors, in addition to immune activation caused by environmental factors, account for the elevated expression of CCR5 and CXCR4 on CD4+ cells of ETH. This increased HIV coreceptor expression may make ETH more susceptible to HIV infection and may account in part for the rapid spread of AIDS in Ethiopia and the rest of Africa as well.
AB - HIV coreceptors play a major role in determining susceptibility and HIV cell tropism. The present work studied whether the high expression of these coreceptors found on lymphocytes and monocytes of Ethiopian immigrants to Israel (ETH) is the result of environmental and/or constitutive genetic factors. The study of 26 ETH shortly after their arrival to Israel (new ETH), 22 ETH in Israel over 7 years (old ETH), and 20 Caucasian Israelis (non-ETH) enabled us to address this issue. The new ETH had elevated levels of activated HLA-DR+CD4+ and CD38+CD8+ cells in comparison with both old ETH and non-ETH groups (P < 0.01), most probably related to chronic helminthic infections. Surface CCR5 expression, i.e., the percentage of CCR5+ cells and the number of CCR5 molecules/cell, was higher (2- to 3- and 8- to 31-fold, respectively) in activated than in nonactivated CD4+ cells, in all groups. However, CCR5 expression, in both activated and nonactivated CD4+ cells, was higher in both ETH groups than in the non-ETH group. CXCR4 expression was higher in nonactivated CD4+ cells in all groups and was also higher in both ETH groups, in both activated and nonactivated CD4+ cells, than in the non-ETH group. These findings suggest that constitutive factors, in addition to immune activation caused by environmental factors, account for the elevated expression of CCR5 and CXCR4 on CD4+ cells of ETH. This increased HIV coreceptor expression may make ETH more susceptible to HIV infection and may account in part for the rapid spread of AIDS in Ethiopia and the rest of Africa as well.
KW - Africa
KW - CCR5
KW - CXCR4
KW - Ethiopians
KW - Immune activation
KW - Susceptibility for HIV infection
UR - http://www.scopus.com/inward/record.url?scp=0034976871&partnerID=8YFLogxK
U2 - 10.1006/clim.2001.5040
DO - 10.1006/clim.2001.5040
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C2 - 11414751
AN - SCOPUS:0034976871
SN - 1521-6616
VL - 100
SP - 107
EP - 117
JO - Clinical Immunology
JF - Clinical Immunology
IS - 1
ER -