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Infection and Immunity, November 2003, p. 6668-6671, Vol. 71, No. 11
0019-9567/03/$08.00+0     DOI: 10.1128/IAI.71.11.6668-6671.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.

Increased Density of Human Immunodeficiency Virus Type 1 Coreceptors CCR5 and CXCR4 on the Surfaces of CD4⁺ T Cells and Monocytes of Patients with Schistosoma mansoni Infection

W. Evan Secor,^1* Amil Shah,² Pauline M. N. Mwinzi,² Bryson A. Ndenga,² Caroline O. Watta,² and Diana M. S. Karanja²

Division of Parasitic Diseases, National Center for Infectious Diseases, Centers for Disease Control and Prevention, Public Health Service, U.S. Department of Health and Human Services, Atlanta, Georgia 30341,¹ Centre for Vector Biology and Control Research, Kenya Medical Research Institute, Kisumu, Kenya²

Received 15 May 2003/ Returned for modification 18 June 2003/ Accepted 8 August 2003

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Distribution of chemokine receptors CCR5 and CXCR4, which are also coreceptors for human immunodeficiency virus type 1 invasion of cells, was measured on the surfaces of CD4⁺ T cells and monocytes in peripheral blood samples from a group of Kenyan car washers. Patients with active schistosomiasis displayed higher cell surface densities of these receptors than did cured schistosomiasis patients.

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Sub-Saharan Africa represents 10% of the world's population but more than 70% of the world's cases of AIDS (16). While many contributing factors have been proposed to explain this phenomenon (1, 2, 4, 5, 19), no clear answer has yet emerged. A prominent hypothesis is that other infections common in Africa, such as parasitic diseases, predispose persons to more readily become infected with human immunodeficiency virus type 1 (HIV-1) if they are exposed to the virus and/or that coinfections exacerbate HIV-1 replication (1, 2). However, direct evaluation of this hypothesis is difficult from both an ethical and logistical perspective. Therefore, to date, studies have utilized either in vitro or indirect in vivo study designs to understand what effect parasitic infections may have on transmission of HIV-1 or progression of AIDS.

One mechanism affecting cellular susceptibility to HIV-1 infection is the differential expression of chemokine receptors that also serve as coreceptors for viral entry into cells (10, 12, 14, 15). Higher cellular expression of the chemokine receptors CXCR4 and CCR5 confer greater susceptibility of cells to in vitro infection with HIV-1. Therefore, we wished to test whether schistosomiasis had any effect on the expression of these chemokine receptors on the surfaces of CD4⁺ peripheral blood T cells and monocytes of patients. To do this, we worked with a previously described cohort of male car washers in Kisumu, Kenya, where HIV-1 seroprevalence approaches 35% in sexually active adults (8, 9, 11). This study was approved by the Scientific Steering Committee of the Kenya Medical Research Institute, the Kenya National Ethical Review Committee, and the Institutional Review Board of the Centers for Disease Control and Prevention.

Inclusion criteria for this study were as follows: patient age of 18 years, current or previous Schistosoma mansoni infection, and willingness to be tested for HIV-1-specific antibodies. Pre- and posttest counseling were provided to patients who gave informed consent. Stool exams were performed by using the Kato Katz technique (Helm TecR P & D Pesquisa E Desenvolmento Ltd., Belo Horizonte, Brazil). Duplicate slides from each of three stool samples collected on consecutive days were examined to determine the mean number of schistosome eggs per gram for each individual. Peripheral blood samples were collected by venipuncture into heparin-coated Vacutainer tubes (Becton Dickinson, Rutherford, N.J.) and immediately transported to the laboratory for processing.

Cells were stained with Cy-Chrome anti-CD4, phycoerythrin-conjugated CD3 or CD14, and fluorescein isothiocyanate-conjugated CCR5 or CXCR4 (all from BD Pharmingen, San Diego, Calif.) for 30 min at 4°C in the dark. For controls, cells were stained with isotype- and fluorochrome-matched antibodies (BD Pharmingen). Following staining, red blood cells were lysed with fluorescence-activated cell sorting (FACS) lysing solution (Becton Dickinson) according to the manufacturer's instructions. After a washing step, cells were fixed using 4% paraformaldehyde in phosphate-buffered saline. Staining was assessed with a FACScaliber flow cytometer (Becton Dickinson) using Cell Quest software for analysis. CD4⁺ cells were gated, and the percent and mean channel fluorescence (MCF) of CCR5 and CXCR4 were determined for CD3⁺ cells (T cells) or CD14⁺ cells (monocytes). The flow cytometer was calibrated every day before samples were run by using four-color Calibrite beads (BD Pharmingen) to ensure that instrument settings were appropriate. In addition, for every fluorochrome-labeled antibody used, an isotype-matched control was included to control for nonspecific antibody staining.

In initial studies, we evaluated chemokine receptor expression on the surfaces of cells from HIV-1-negative individuals to avoid any independent effects HIV-1 may have had on the expression of CCR5 or CXCR4. Statistical comparisons were made by using the nonparametric Mann-Whitney test. When we compared the density (MCF) of CCR5 and CXCR4 on the surfaces of CD4⁺ CD3⁺ and CD4⁺ CD14⁺ cells, we found that patients with active schistosomiasis expressed significantly higher levels of CXCR4 on the surfaces of both T cells and monocytes compared to persons who had previously had schistosomiasis but had been treated (Table 1). In contrast, the percentages of cells positive for CXCR4 were similar for the two groups of patients (data not shown), suggesting that the density, but not distribution, of these receptors was altered by schistosomiasis. CCR5 MCF levels and percent CCR5 cells were elevated in patients with active schistosomiasis, but the values for the two groups were not significantly different (Table 1 and data not shown).

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TABLE 1. Chemokine receptor expression of patients with active schistosomiasis compared to cured schistosomiasis patients

To extend these studies, we also evaluated the chemokine receptor profiles before and after treatment of individual patients. In this portion of the study, we included both HIV-1-positive and -negative individuals to determine whether the beneficial effect of treating schistosomiasis led to a reduction in chemokine receptor density irrespective of HIV-1 infection status. The median time between sampling when patients were actively infected and after they had no schistosome eggs was 11 months (range, 4 to 14 months). Figure 1 shows the chemokine receptor staining profiles of CD4⁺ T cells from a representative patient during active schistosomiasis and after the patient was cured. Posttreatment levels of both CCR5 and CXCR4 on the surfaces of CD4⁺ CD3⁺ cells were significantly lower than pretreatment levels (Fig. 2). Cells from HIV-1-negative and HIV-1-positive patients showed a decrease in the MCF of chemokine receptors after treatment for schistosomiasis. There was no clear association between the length of time after treatment and decrease in chemokine receptor expression, although the patient who had been clear of schistosomiasis for only 4 months demonstrated the smallest decrease in CCR5 MCF and was the only patient to show a marked increase in CXCR4 MCF. Median MCF values for CCR5 and CXCR4 expression on monocytes also decreased after treatment, but the differences were not statistically significant (Fig. 2).

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FIG. 1. Comparison of chemokine receptor staining profiles for a patient during active schistosomiasis and after the patient was cured. MCF values for CCR5 and CXCR4 were calculated for the population of CD4 cells that was also positive for CD3, as represented by the rectangular box in the right half of each profile. Abbreviations: Pre-Rx and Post-Rx, before and after treatment for schistosomiasis, respectively; FITC, fluorescein isothiocyanate; PE, phycoerythrin; ISO, isotype.

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FIG. 2. Chemokine receptor expression of patients before and after treatment for schistosomiasis. MCF data for chemokine receptors minus the MCF of the isotype control for individuals before (Pre-Rx) and after (Post-Rx) treatment with praziquantel are shown. Data from HIV-1-negative individuals (solid lines) and HIV-1-positive patients (broken lines) are shown. The numbers in parentheses below the graph are the median values for the group. Statistical analyses were performed by using the nonparametric Wilcoxon matched-pair signed-rank test. The MCF group medians (quartiles shown in parentheses [25th quartile; 75th quartile]) for the isotope controls were as follows: on the surface of CD4+ CD3+ cells, 20.8 (18.3; 23.2) for individuals with schistosome eggs and 20.9 (17.1; 23.9) for individuals with no schistosome eggs; on the surface of CD4+ CD14+ cells, 46.6 (33.0; 66.2) for individuals with schistosome eggs and 57.4 (34.0; 72.2) for individuals with no schistosome eggs. The isotype control MCF values were not significantly different for either cell type.

Increased density of CXCR4 and CCR5 on the surfaces of cells from patients with schistosomiasis is consistent with observations that their expression is upregulated by the Th2-associated cytokines interleukin-4 (3, 17) and interleukin-10 (14, 18), respectively, which are commonly produced in response to helminth infections such as schistosomiasis. Because a higher number of chemokine receptors on the surfaces of CD4⁺ cells is associated with increased infection by HIV-1 (10, 12, 14, 15), these results imply that cells from schistosomiasis patients may be more susceptible to infection with HIV-1 and that chemotherapy for schistosomiasis may reduce the susceptibility of the patient to the virus if the patient is exposed to the virus. The reduction of HIV-1 coreceptor densities on the surfaces of CD4⁺ T cells from HIV-1-positive schistosomiasis patients also suggests that praziquantel treatment may provide a beneficial effect in terms of the progression of a coinfected patient to AIDS. Analogous observations of increased chemokine receptor density have previously been made in patients with generalized helminthiasis (7). These patients also had increased in vitro susceptibility to HIV-1 (13). Similarly, treatment of filariasis patients reduced the susceptibility of their cells to infection with HIV-1 in vitro (6). While it is clearly not possible to definitively conclude from these results that helminth infections confer a greater risk for contracting HIV or AIDS, these data do support the hypothesis that the public health advantages of antihelminthic treatment for persons at risk of HIV or AIDS may go beyond the simple benefit of curing their parasitic infections (1, 2).

 
This manuscript is published with the permission of the director of the Kenya Medical Research Institute and supported in conjunction with the VAMC Atlanta and the Atlanta Research and Education Foundation.

We thank Daniel G. Colley for helpful discussions, Patrick J. Lammie for critical reading of the manuscript, and Jose Stout for flow cytometer access. We also thank Julius Andove, Kennedy Matunda, and Nathan Mulonga for expert field assistance.

 
* Corresponding author. Mailing address: Immunology Branch, Division of Parasitic Diseases, Centers for Disease Control and Prevention, 4770 Buford Highway, NE, MS-F13, Atlanta, GA 30341-3724. Phone: (770) 488-4115. Fax: (770) 488-4108. E-mail: was4{at}cdc.gov.

Editor: J. M. Mansfield

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Infection and Immunity, November 2003, p. 6668-6671, Vol. 71, No. 11
0019-9567/03/$08.00+0     DOI: 10.1128/IAI.71.11.6668-6671.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.

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