Journal of Clinical Microbiology, October 2000, p. 3903-3904, Vol. 38, No. 10
0095-1137/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Human T-Cell Lymphotropic Virus Type I Association with
Strongyloïdes stercoralis: a Case Control Study
among Caribbean Blood Donors from Guadeloupe (French West Indies)
In tropical or subtropical areas such as Southern Japan, the
Caribbean, Central and South America, both human T-cell lymphotropic virus type I (HTLV-I) and Strongyloides stercoralis
infection are endemic (4, 8). Several studies have
documented an unexpectedly high prevalence of S. stercoralis
in HTLV-I carriers and of HTLV-I among S. stercoralis
carriers. The links between two such taxonomically distant infectious
agents remain unclear and controversial. Japanese S. stercoralis carriers were found to have a significantly higher seroprevalence for HTLV-I than non-S. stercoralis carriers
(5). But conversely, Jamaican HTLV-I carriers did not
exhibit higher rates for S. stercoralis antibodies than
HTLV-I negative subjects (6). In Guadeloupe, a French West
Indian island, HTLV-I is endemic (9), whereas parasitic
diseases, with the only exception of S. stercoralis
infection, have been largely eradicated in the last 20 years. We
conducted a case control study among healthy blood donors in order to
determine if HTLV-I infection is associated with S. stercoralis carriage. In Guadeloupe, subjects have to fulfill the
French criteria for blood donation, i.e., fully informed consent, free
donation, systematic pretest interview, and clinical examination; the
sex ratio of Guadeloupean blood donors is about 1:1, and the mean age
is 32 years (range, 18 to 65 years).
We compared the frequency of Strongyloides antibody
detection among 119 HTLV-I-positive blood donors (85 females with a
mean age of 49 ± 26 years and 34 males with a mean age of 49 ± 28 years) with that of 119 HTLV-I-negative blood donors (68 females
with a mean age of 33 ± 22 years and 51 males with a mean age of 34 ± 22 years). Controls did not significantly differ with regard to age and
sex from the general blood donor population. All of these subjects had
been systematically screened for HTLV-I as blood donors (HTLV-I Enzymo
Immuno Assay 2.0 Abbott) and confirmed positive for the case group
(HTLV I/II WB 2.4 Genelabs). They were also blindly assessed for
S. stercoralis antibodies by indirect immunofluorescence
using Strongyloides ratti larval antigens, with a positive
threshold titer set at 1/60 (3).
As shown in Table 1, a significant
association was found between HTLV-I infection and S. stercoralis serological results. In total, 31.1% of HTLV-I
positive subjects were found to have S. stercoralis
antibodies, as compared to 10.9% of negative donors (age-adjusted odds
ratio [OR], 2.08; confidence interval [CI], 1.0 to 4.35). The
association appeared significant only in female (age-adjusted OR,
7.50; CI, 2.20 to 25.80), not in male (OR, 1.79; CI, 0.59 to 5.42),
subjects.
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LETTER
TABLE 1.
Parasitic seroprevalence and association between HTLV-I
infection and S. stercoralis
antibodies
In conclusion, this is the first report highlighting the association between HTLV-I infection and S. stercoralis antibody asymptomatic carriage. The male-female difference in the magnititude of the ORs should be interpreted with caution, as the number of male subjects was limited. Further epidemiological studies are necessary to examine in detail whether other factors such as socioeconomic status could interact with the HTLV-I-S. stercoralis association. Although some hypotheses have been put forward, such as virus-induced immune deficiency or the promotion of HTLV-I infection by the parasite (1, 7), the relation between the retrovirus HTLV-I and the worm S. stercoralis remains puzzling and needs further study. The possible relation is not purely speculative but has clinical implications, since both enhanced morbidity-mortality and treatment failures in dually infected subjects have been reported (2). Furthermore, the lack of efficient antiviral drugs for HTLV-I offers limited management options. However, once HTLV-I and strongyloidiasis have been identified by screening, the monitoring of both, and the thoroughly treatment of strongyloidiasis, can be helpful clinically.
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FOOTNOTES |
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* Phone: 0590.89.12.70. Fax: 0590.89.11.56 E-mail: gery.courouble{at}wanadoo.fr
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REFERENCES |
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| 6. | Neva, F. A., E. L. Murphy, A. Gam, B. Hanchard, J. P. Figueroa, and W. A. Blattner. 1989. Antibodies to Strongyloïdes stercoralis in healthy Jamaican carriers of HTLV-I. N. Engl. J. Med. 320:252-253[Medline]. |
| 7. | Neva, F. A., J. O. Filho, A. A. Gam, R. Thompson, V. Freitas, A. Melo, and E. M. Carvalho. 1998. Interferon-gamma and interleukine-4 responses in relation to serum IgE levels in persons infected with human T lymphotropic virus type I and Strongyloides stercoralis. J. Infect. Dis. 178:1856-1859[CrossRef][Medline]. |
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| 9. | Rouet, F., R. Rabier, C. Foucher, B. Chancerel, F. Agis, and M. Strobel. 1999. Geographical clustering of human T-cell lymphotrophic virus type I in Guadeloupe, an endemic caribbean area. Int. J. Cancer 81:330-334[CrossRef][Medline]. |
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Géry Courouble* François Rouet Cécile Herrmann-Storck Muriel Nicolas Laboratoire de Parasitologie C.H.U. de Pointe-à-Pitre Pointe-à-Pitre Guadeloupe, France | |||||
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Ermanno Candolfi Institut de Parasitologie et de Pathologie Tropicale Strasbourg, France | |||||
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Michel Strobel Service Maladies Infectieuses C.H.U. de Pointe-à-Pitre Pointe-à-Pitre, Guadeloupe, France | |||||
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Bernard Carme Service de Parasitologie-Mycologie Equipe JE 21-88 Cayenne Guyane, France |
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