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Spatial clustering of filarial transmission before and after a Mass Drug Administration in a setting of low infection prevalence

BACKGROUND: In the global program for the elimination of lymphatic filariasis (LF) longitudinal assessment of the prevalence of microfilaremia and antigenemia is recommended to monitor the effect of mass treatment on transmission. Additional monitoring tools such as entomologic and antibody methods...

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Autores principales: Washington, Charles H, Radday, Jeanne, Streit, Thomas G, Boyd, Heather A, Beach, Michael J, Addiss, David G, Lovince, Rodrigue, Lovegrove, Maribeth C, Lafontant, Jack G, Lammie, Patrick J, Hightower, Allen W
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC420477/
https://www.ncbi.nlm.nih.gov/pubmed/15128461
http://dx.doi.org/10.1186/1475-2883-3-3
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author Washington, Charles H
Radday, Jeanne
Streit, Thomas G
Boyd, Heather A
Beach, Michael J
Addiss, David G
Lovince, Rodrigue
Lovegrove, Maribeth C
Lafontant, Jack G
Lammie, Patrick J
Hightower, Allen W
author_facet Washington, Charles H
Radday, Jeanne
Streit, Thomas G
Boyd, Heather A
Beach, Michael J
Addiss, David G
Lovince, Rodrigue
Lovegrove, Maribeth C
Lafontant, Jack G
Lammie, Patrick J
Hightower, Allen W
author_sort Washington, Charles H
collection PubMed
description BACKGROUND: In the global program for the elimination of lymphatic filariasis (LF) longitudinal assessment of the prevalence of microfilaremia and antigenemia is recommended to monitor the effect of mass treatment on transmission. Additional monitoring tools such as entomologic and antibody methods may be useful in identifying residual foci of infection. In this study, we characterized serologic markers of infection and exposure spatially both before and after mass treatment, in an area of initial low Wuchereria bancrofti infection prevalence. METHODS: Consenting persons in the sentinel community were tested for circulating microfilaria and antigen (by immunochromatographic test) before and after the 1(st )annual mass drug administration of diethylcarbamazine and albendazole. A cohort of 161 persons provided serum specimens both years that were tested for antifilarial IgG (1 and 4) antibody. Every house was mapped using a differential Global Positioning System; this information was linked to the serologic data. W. bancrofti infection in the mosquito vector was assessed with year-round collection. Multiple linear regression was used to investigate the influence of antigen-positive persons on the antifilarial antibody responses of antigen-negative neighbors. RESULTS: After mass treatment, decreases were observed in the sentinel site in the overall prevalence of antigen (10.4% to 6.3%) and microfilaremia (0.9 to 0.4%). Of the persons in the cohort that provided serum specimens both years, 79% received treatment. Antigen prevalence decreased from 15.0% to 8.7%. Among 126 persons who received treatment, antigen and antifilarial IgG1 prevalence decreased significantly (p = 0.002 and 0.001, respectively). Among 34 persons who did not receive treatment, antifilarial IgG1 prevalence increased significantly (p = 0.003). Average antifilarial IgG1 levels decreased in households with high treatment coverage and increased in households that refused treatment. Each 10-meter increase in distance from the residence of a person who was antigen-positive in 2000 was associated a 4.68 unit decrease in antifilarial IgG1 level in 2001, controlling for other factors (p = 0.04). DISCUSSION: Antifilarial antibody assays can be used as a measure of filarial exposure. Our results suggest that micro-scale spatial heterogeneity exists in LF exposure and infection. Treatment appeared to be associated with reduced exposure at the sub-community level, suggesting the need to achieve high and homogeneous coverage. Public health messages should note the benefits of having one's neighbors receive treatment with antifilarial drugs.
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spelling pubmed-4204772004-06-11 Spatial clustering of filarial transmission before and after a Mass Drug Administration in a setting of low infection prevalence Washington, Charles H Radday, Jeanne Streit, Thomas G Boyd, Heather A Beach, Michael J Addiss, David G Lovince, Rodrigue Lovegrove, Maribeth C Lafontant, Jack G Lammie, Patrick J Hightower, Allen W Filaria J Research BACKGROUND: In the global program for the elimination of lymphatic filariasis (LF) longitudinal assessment of the prevalence of microfilaremia and antigenemia is recommended to monitor the effect of mass treatment on transmission. Additional monitoring tools such as entomologic and antibody methods may be useful in identifying residual foci of infection. In this study, we characterized serologic markers of infection and exposure spatially both before and after mass treatment, in an area of initial low Wuchereria bancrofti infection prevalence. METHODS: Consenting persons in the sentinel community were tested for circulating microfilaria and antigen (by immunochromatographic test) before and after the 1(st )annual mass drug administration of diethylcarbamazine and albendazole. A cohort of 161 persons provided serum specimens both years that were tested for antifilarial IgG (1 and 4) antibody. Every house was mapped using a differential Global Positioning System; this information was linked to the serologic data. W. bancrofti infection in the mosquito vector was assessed with year-round collection. Multiple linear regression was used to investigate the influence of antigen-positive persons on the antifilarial antibody responses of antigen-negative neighbors. RESULTS: After mass treatment, decreases were observed in the sentinel site in the overall prevalence of antigen (10.4% to 6.3%) and microfilaremia (0.9 to 0.4%). Of the persons in the cohort that provided serum specimens both years, 79% received treatment. Antigen prevalence decreased from 15.0% to 8.7%. Among 126 persons who received treatment, antigen and antifilarial IgG1 prevalence decreased significantly (p = 0.002 and 0.001, respectively). Among 34 persons who did not receive treatment, antifilarial IgG1 prevalence increased significantly (p = 0.003). Average antifilarial IgG1 levels decreased in households with high treatment coverage and increased in households that refused treatment. Each 10-meter increase in distance from the residence of a person who was antigen-positive in 2000 was associated a 4.68 unit decrease in antifilarial IgG1 level in 2001, controlling for other factors (p = 0.04). DISCUSSION: Antifilarial antibody assays can be used as a measure of filarial exposure. Our results suggest that micro-scale spatial heterogeneity exists in LF exposure and infection. Treatment appeared to be associated with reduced exposure at the sub-community level, suggesting the need to achieve high and homogeneous coverage. Public health messages should note the benefits of having one's neighbors receive treatment with antifilarial drugs. BioMed Central 2004-05-05 /pmc/articles/PMC420477/ /pubmed/15128461 http://dx.doi.org/10.1186/1475-2883-3-3 Text en Copyright © 2004 Washington et al; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.
spellingShingle Research
Washington, Charles H
Radday, Jeanne
Streit, Thomas G
Boyd, Heather A
Beach, Michael J
Addiss, David G
Lovince, Rodrigue
Lovegrove, Maribeth C
Lafontant, Jack G
Lammie, Patrick J
Hightower, Allen W
Spatial clustering of filarial transmission before and after a Mass Drug Administration in a setting of low infection prevalence
title Spatial clustering of filarial transmission before and after a Mass Drug Administration in a setting of low infection prevalence
title_full Spatial clustering of filarial transmission before and after a Mass Drug Administration in a setting of low infection prevalence
title_fullStr Spatial clustering of filarial transmission before and after a Mass Drug Administration in a setting of low infection prevalence
title_full_unstemmed Spatial clustering of filarial transmission before and after a Mass Drug Administration in a setting of low infection prevalence
title_short Spatial clustering of filarial transmission before and after a Mass Drug Administration in a setting of low infection prevalence
title_sort spatial clustering of filarial transmission before and after a mass drug administration in a setting of low infection prevalence
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC420477/
https://www.ncbi.nlm.nih.gov/pubmed/15128461
http://dx.doi.org/10.1186/1475-2883-3-3
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