Herramientas no invasivas en Venezuela: comparación entre las pruebas inmunoserológicas DAT, rK26 y rK39 en el diagnóstico de leishmaniasis visceral
Keywords:
leishmaniasis visceral/diagnóstico, pruebas de aglutinación, prueba ELISA, cromatografía en papel, Leishmania infantum, humanos, Venezuela
Abstract
Introducción. La leishmaniasis visceral constituye un problema de salud pública en los países en donde es endémica por ser potencialmente letal, principalmente en niños. El diagnóstico rápido es importante en el control de la enfermedad.Objetivo. Comparar las pruebas inmunocromatográficas rK39 (rK39 dipstick, Kalazar detect test, Inbios Internacional Inc.), ELISA rK26 y la prueba de aglutinación directa (Kit Biomedical Research) en relación con la prueba de ELISA rK39, como herramientas serodiagnósticas para la leishmaniasis visceral en Venezuela.
Materiales y métodos. Se estudiaron 50 muestras séricas de pacientes positivos por la prueba ELISA rK39, provenientes de diferentes zonas endémicas: Nueva Esparta, Lara, Anzoátegui y Trujillo; se incluyeron 17 muestras de voluntarios sanos y 25 de pacientes con otras enfermedades. Se utilizó la prueba ELISA rK39 como método de referencia, considerándola como patrón de referencia imperfecto, a partir del cual se determinaron los valores de sensibilidad, especificidad, razón de verosimilitud y valores diagnóstico positivo y negativo en las demás pruebas evaluadas.
Resultados. Todas las pruebas mostraron una fuerte correlación (p<0,0001) con la ELISA rK39. La aglutinación directa y la prueba inmunocromatográfica rK39 presentaron altos valores de sensibilidad, 89,74% (IC95% 81,34-98,15) y 94,15% (IC95% 87,65-100), respectivamente, y de especificidad, 81% (IC95% 79,96-99,51) y 100% (IC95% 100-100). La prueba ELISA rK26, a pesar de poseer buena especificidad, 99% (IC95% 95,17-100), tuvo baja sensibilidad, 37% (IC95% 23,41-50,15).
Conclusión. Las pruebas de aglutinación directa y la prueba inmunocromatográfica rK39 presentaron los mayores valores de sensibilidad y especificidad. Ambas son simples, económicas y fácilmente aplicables. Por ello, son recomendables para efectuar un diagnóstico de leishmaniasis visceral eficaz y precoz en Venezuela.
Downloads
Download data is not yet available.
References
1. Kafetzis DA, Maltezou HC. Visceral leishmaniasis in pediatrics. Curr Opin Infect Dis. 2002;15:289-94.
2. Palatnik-de-Sousa CB, dos Santos WR, França-Silva JC, da Costa RT, Reis AB, Palatnik M, et al. Impact of canine control on the epidemiology of canine and human visceral Leishmaniasis in Brazil. Am J Trop Med Hyg. 2001;65:510-7.
3. Zerpa O, Ulrich M, Borges R, Rodríguez V, Centeno M, Negron E, et al. Epidemiological aspects of human and canine visceral leishmaniasis in Venezuela. Rev Panam Salud Pública. 2003;13:239-45.
4. WHO. Zoonoses and veterinary public health: Leishmaniasis [online]. Fecha de consulta: 15 de agosto de 2007]. Disponible en: http://www.who.int/zoonoses/diseases/leishmaniasis/en/.
5. OPS. Definiciones de caso: leishmaniasis visceral. Boletín Epidemiológico. 2002;23:14.
6. Sundar S, Rai M. Laboratory diagnosis of visceral leishmaniasis. Clin Diagn Lab Immunol. 2002;9:951-8.
7. Andrade CR, Nascimento AE, Moura PM, Andrade PP. Leishmania donovani donovani and Leishmania donovani chagasi as antigens in a direct agglutination assay for the diagnosis of kala-azar. Braz J Med Biol Res.1989;22:611-5.
8. De Assis TS, Braga AS, Pedras MJ, Barral AM, Siquera IC, Costa CHN, et al. Validation of the rapid immunochromatographic test IT-LEISH® for the diagnosis of human visceral leishmaniasis. Epidemiol Serv Saude. 2008;17:112-6.
9. Delgado O, Feliciangeli MD, Coraspe V, Silva S, Pérez A, Arias J. Value of a dipstick based on recombinantrK39 antigen for differential diagnosis of American visceral leishmaniasis from other sympatric endemic diseases in Venezuela. Parasite. 2001;8:355-7.
10. Garcez LM, Shaw JJ, Silveira FT. Direct agglutination tests in the serodiagnosis of visceral leishmaniasis in the state of Para. Rev Soc Bras Med Trop. 1996;29:165-80.
11. Pedras MJ, de Gouvêa Viana L, de Oliveira EJ, Rabello A. Comparative evaluation of direct agglutination test rK39 and soluble antigen ELISA and IFAT for the diagnosis of visceral leishmaniasis. Trans R Soc Trop Med Hyg. 2008;102:172-8.
12. Terán-Angel G, Schallig HD, Zerpa O, Rodríguez V, Ulrich M, Cabrera M. The direct agglutination test as an alternative method for the diagnosis of canine and human visceral leishmaniasis. Biomédica. 2007;27:447-53.
13. El Harith A, Kolk AH, Leeuwenburg J, Muigai R, Huigen E, Jelsma T, et al. Improvement of a direct agglutination test for field studies of visceral leishmaniasis. J Clin Microbiol.1988;26:1321-5.
14. Meredith SE, Kroon NC, Sondorp E, Seaman J, Goris MG, van Ingen CW, et al. Leish-KIT, a stable direct agglutination test based on freeze-dried antigen for serodiagnosis of visceral leishmaniasis. J Clin Microbiol.1995;33:1742-5.
15. Oskam L, Nieuwenhuijs JL, Hailu A. Evaluation of the direct agglutination test (DAT) using freeze-dried antigen for the detection of anti-Leishmania antibodies in stored sera from various patient groups in Ethiopia. Trans R Soc Trop Med Hyg.1999;93:275-7.
16. Valenstein PN. Evaluating diagnostic tests with imperfect standards. Am J Clin Pathol.1990;93:252-8.
17. Burns JM, Shreffler WG, Benson DR, Ghalib HW, Badaro R, Reed SG. Molecular characterization of a kinesin-related antigen of Leishmania chagasi that detects specific antibody in African and American visceral leishmaniasis. Proc Natl Acad Sci USA. 1993;90:775-9.
18. Salotra P, Sreenivas G, Beena KR, Mukherjee A, Ramesh V. Parasite detection in patients with post kala-azar dermal leishmaniasis in India: a comparison between molecular and immunological methods. J Clin Pathol. 2003;56:840-3.
19. Singh S, Kumari V, Singh N. Predicting kala-azar disease manifestations in asymptomatic patients with latent Leishmania donovani infection by detection of antibody against recombinant K39 antigen. Clin Diagn Lab Immunol. 2002;9:568-72.
20. Sreenivas G, Ansari NA, Singh R, Subba BV, Bhatheja R, Negi NS, et al. Diagnosis of visceral leishmaniasis: comparative potential of amastigote antigen, recombinant antigen and PCR. Br J Biomed Sci. 2002;59:218-22.
21. Ozensoy S, Ozbel Y, Turgay N, Alkan MZ, Gul K, Gilman-Sachs A, et al. Serodiagnosis and epidemiology of visceral leishmaniasis in Turkey. Am J Trop Med Hyg. 1998;59:363-9.
22. Qu JQ, Zhong L, Masoom-Yasinzai M, Abdur-Rab M, Aksu HS, Reed SG, et al. Serodiagnosis of Asian leishmaniasis with a recombinant antigen from the repetitive domain of a Leishmania kinesin. Trans R Soc Trop Med Hyg. 1994;8:543-5.
23. Zijlstra EE, Daifalla NS, Kager PA, Khalil EA, El-Hassan AM, Reed SG, et al. rK39 enzyme-linked immunosorbent assay for diagnosis of Leishmania donovani infection. Clin Diagn Lab Immunol. 1998;5:717-20.
24. Altman DG. Practical statistics for medical research. London: Chapman & Hall Press; 1991. p. 611.
25. Murray HW. Treatment of visceral leishmaniasis in 2004. Am J Trop Med Hyg. 2004;71:787-94.
26. Chulay JD, Bryceson AD. Quantitation of amastigotes of Leishmania donovani in smears of splenic aspirates from patients with visceral leishmaniasis. Am J Trop Med Hyg. 1983;32:475-9.
27. Hailu A, Musa AM, Royce C, Wasunna M. Visceral leishmaniasis: new health tools are needed. PLoS Med. 2005;2:e211.
28. Singh RK, Pandey HP, Sundar S. Visceral leishmaniasis (kala-azar): challenges ahead. Indian J Med Res. 2006;123:331-44.
29. Chappuis F, Rijal S, Soto A, Menten J, Boelaert M. A meta-analysis of the diagnostic performance of the direct agglutination test and rK39 Kalazar detect test for visceral leishmaniasis. BMJ. 2006;333:723.
30. Joshi AB, Singhasivanon P, Khusmith S, Fungladda W, Nandy A. Evaluation of direct agglutination test (DAT) as an immunodiagnostic tool for diagnosis of visceral leishmaniasis in Nepal. Southeast Asian J Trop Med Public Health.1999;30:583-5.
31. Carvalho SF, Lemos EM, Corey R, Dietze R. Performance of recombinant K39 antigen in the diagnosis of Brazilian visceral leishmaniasis. Am J Trop Med Hyg. 2003;68:321-4.
32. Sundar S, Reed SG, Singh VP, Kumar PC, Murray HW. Rapid accurate field diagnosis of Indian visceral leishmaniasis. Lancet. 1998;351:563-5.
33. Goswami RP, Bairagi B, Kundu PK. K39 strip test-easy, reliable and cost-effective field diagnosis for visceral leishmaniasis in India. J Assoc Physicians India. 2003;51:759-61.
34. Bhatia A, Daifalla NS, Jen S, Badaro R, Reed SG, Skeiky YA. Cloning, characterization and serological evaluation of K9 and K26: two related hydrophilic antigens of Leishmania chagasi. Mol Biochem Parasitol.1999;102:249-61.
35. Da Costa RT, Franca JC, Mayrink W, Nascimento E, Genaro O, Campos-Neto A. Standardization of a rapid immunochromatographic test with the recombinant antigens K39 and K26 for the diagnosis of canine visceral leishmaniasis. Trans R Soc Trop Med Hyg. 2003;97:678-82.
36. De Almeida L, Romero HD, Prata A, Costa RT, Nascimento E, Carvalho SF, et al. Immunologic tests in patients after clinical cure of visceral leishmaniasis. Am J Trop Med Hyg. 2006;75:739-43.
How to Cite
1.
Terán-Ángel G, Rodríguez V, Silva R, Zerpa O, Schallig H, Ulrich M, et al. Herramientas no invasivas en Venezuela: comparación entre las pruebas inmunoserológicas DAT, rK26 y rK39 en el diagnóstico de leishmaniasis visceral. Biomed. [Internet]. 2010 Mar. 1 [cited 2026 Jan. 14];30(1):39-45. Available from: https://revistabiomedicaorg.biteca.online/index.php/biomedica/article/view/151
Some similar items:
- Clemencia Ovalle-Bracho, Carolina Camargo, Yira Díaz-Toro, Marcela Parra-Muñoz, Molecular typing of Leishmania (Leishmania) amazonensis and species of the subgenus Viannia associated with cutaneous and mucosal leishmaniasis in Colombia: A concordance study , Biomedica: Vol. 38 No. 1 (2018)
- Ana M. Montalvo, Jorge Fraga, Ivón Montano, Lianet Monzote, Gert Van der Auwera, Marcel Marín, Carlos Muskus, Molecular identification of Leishmania spp. clinical isolates from Colombia based on hsp70 gene , Biomedica: Vol. 36 (2016): Suplemento 1, Microbiología médica
- Manuel Toquero, Antonio Morocoima, Elizabeth Ferrer, Seroprevalence and risk factors of cysticercosis in two rural communities in Anzoátegui state, Venezuela , Biomedica: Vol. 37 No. Sup.1 (2017): Suplemento 1, Alteraciones del sistema nervioso
- Olga L. Cabrera, Leonard E. Munstermann, Rocío Cárdenas, Cristina Ferro, PCR as a tool in confirming the experimental transmission of Leishmania chagasi to hamsters by Lutzomyia longipalpis (Diptera:Psychodidae). , Biomedica: Vol. 23 No. 2 (2003)
- Camilo Andrés Morales, Juliana Palacio, Gerzaín Rodríguez, Yenny Carolina Camargo, Zosteriform cutaneous leishmaniasis due to Leishmania (Viannia) panamensis and Leishmania (Viannia) braziliensis: Report of three cases , Biomedica: Vol. 34 No. 3 (2014)
- Elsa Nieves, Neudo Buelvas, Maritza Rondón, Néstor González, The salivary glands of two sand fly vectors of Leishmania: Lutzomyia migonei (França) and Lutzomyia ovallesi (Ortiz) (Diptera: Psychodidae) , Biomedica: Vol. 30 No. 3 (2010)
- Guillermo Terán-Angel, Henk Schallig, Olga Zerpa, Vestalia Rodríguez, Marian Ulrich, Maira Cabrera, The direct agglutination test as an alternative method for the diagnosis of canine and human visceral leishmaniasis , Biomedica: Vol. 27 No. 3 (2007)
- Alberto Tobón, Danger signs in the malaria patient , Biomedica: Vol. 29 No. 2 (2009)
- Marcel Marín, Yudy Alexandra Aguilar, José Robinson Ramírez, Omar Triana, Carlos Enrique Muskus, Molecular and immunological analyses suggest the absence of hydrophilic surface proteins in Leishmania (Viannia) panamensis , Biomedica: Vol. 28 No. 3 (2008)
- Luis Alberto Cortés, Jhon James Fernández, Species of Lutzomyia involved in an urban focus of visceral and cutaneous leishmaniasis , Biomedica: Vol. 28 No. 3 (2008)
Issue
Section
Original articles
| Article metrics | |
|---|---|
| Abstract views | |
| Galley vies | |
| PDF Views | |
| HTML views | |
| Other views | |
Escanea para compartir










