A simple immune complex dissociation ELISA for leishmaniasis: Standardization of the assay in experimental models and preliminary results in canine and human samples

Carregando...
Imagem de Miniatura
Citações na Scopus
23
Tipo de produção
article
Data de publicação
2013
Título da Revista
ISSN da Revista
Título do Volume
Editora
ELSEVIER SCIENCE BV
Autores
CARVALHO, Camila Aparecida de
PARTATA, Anette Kelsei
HIRAMOTO, Roberto Mitsuyoshi
BORBOREMA, Samanta Etel Treiger
NASCIMENTO, Nanci do
Citação
ACTA TROPICA, v.125, n.2, p.128-136, 2013
Projetos de Pesquisa
Unidades Organizacionais
Fascículo
Resumo
Visceral leishmaniasis, caused by Leishmania (Leishmania) chagasi, is a chronic parasitic disease of humans and dogs. Confirmation of the protozoal agent in bone marrow, lymph node or spleen aspirate is diagnostic, while specific-IgG serology is used mainly for epidemiology despite the general presence of high levels of serum immunoglobulin. Anecdotal reports of false-negative serology in active disease cases are known and are ascribed to the formation of immune complexes. Because dissociation of immune complexes can be accomplished by acid treatment, we devised a simple, routine enzyme immunoassay (ELISA) for the dissociation of immune complexes in serum samples using acid treatment in wells adsorbed with Leishmania antigen (dELISA). Confirmatory acid dot-blot was also developed for antigen detection by anti-Leishmania rabbit antiserum. In experimental L. chagasi hamster models, immune complexes interfered with ELISA mostly in the 30 and 60 days postinfection, according to both dELISA and antigen dot-blot results. In larger samples from endemic areas, dELISA was positive in 10% of seronegative dog samples (7/70) and 3.5% in negative human samples (3/88), showing that dELISA could be used in the serodiagnosis of visceral leishmaniasis. Moreover, dELISA could be used as an alternative approach to screening asymptomatic visceral leishmaniasis patients, instead of invasive confirmatory testing.
Palavras-chave
Immune complexes, ELISA, Interference
Referências
  1. Afrin F, 1997, INFECT IMMUN, V65, P2371
  2. Alves Waneska Alexandre, 2004, Cad Saude Publica, V20, P259, DOI 10.1590/S0102-311X2004000100043
  3. Azazy Ahmed Abdulwaly, 2004, Journal of the Egyptian Society of Parasitology, V34, P35
  4. Azazy AA, 1997, ANN TROP MED PARASIT, V91, P153
  5. CARVALHO EM, 1983, AM J TROP MED HYG, V32, P61
  6. CASALI P, 1979, CLIN EXP IMMUNOL, V37, P295
  7. Chappuis F, 2007, NAT REV MICROBIOL, V5, P873, DOI 10.1038/nrmicro1748
  8. Cota GF, 2011, PLOS NEGLECT TROP D, V5, DOI 10.1371/journal.pntd.0001153
  9. Da Silva MRB, 2005, AM J TROP MED HYG, V72, P811
  10. de Valliere S, 2009, AM J TROP MED HYG, V81, P209
  11. Durkin M, 2009, CLIN VACCINE IMMUNOL, V16, P1453, DOI 10.1128/CVI.00227-09
  12. Elshafie AI, 2007, J IMMUNOL, V178, P5383
  13. ElShafie A.I., 2006, AM J TROP MED HYG, V75, P864
  14. EVANS TG, 1988, INFECT IMMUN, V56, P3139
  15. GALVAOCASTRO B, 1981, AM J TROP MED HYG, V30, P1238
  16. Gustaw KA, 2008, J NEUROCHEM, V106, P1350, DOI 10.1111/j.1471-4159.2008.05477.x
  17. Halstead SB, 2010, LANCET INFECT DIS, V10, P712, DOI 10.1016/S1473-3099(10)70166-3
  18. HOLLOWAY Y, 1993, J CLIN MICROBIOL, V31, P3247
  19. Imaz MS, 2008, BRAZ J INFECT DIS, V12, P234, DOI 10.1590/S1413-86702008000300014
  20. Iqbal J, 2002, J CLIN MICROBIOL, V40, P475, DOI 10.1128/JCM.40.2.475-479.2002
  21. KAR K, 1995, CRIT REV MICROBIOL, V21, P123, DOI 10.3109/10408419509113537
  22. Koraka P, 2003, J CLIN MICROBIOL, V41, P4154, DOI 10.1128/JCM.41.9.4154-4159.2003
  23. Kumar R, 2001, CLIN DIAGN LAB IMMUN, V8, P1220, DOI 10.1128/CDLI.8.6.1220-1224.2001
  24. LAMBERT PH, 1981, J CLIN INVEST, V67, P77, DOI 10.1172/JCI110035
  25. LEWIS DE, 1995, CLIN DIAGN LAB IMMUN, V2, P87
  26. Li QY, 2007, BMC NEUROSCI, V8, DOI 10.1186/1471-2202-8-22
  27. Maia Z, 2012, PLOS NEGLECT TROP D, V6, DOI 10.1371/journal.pntd.0001484
  28. MANCIANTI F, 1995, VET PARASITOL, V59, P13, DOI 10.1016/0304-4017(94)00738-X
  29. Margarito JM, 1998, J VET MED B, V45, P263
  30. Miles SA, 2005, J EXP MED, V201, P747, DOI 10.1084/jem.20041470
  31. MILES SA, 1993, NEW ENGL J MED, V328, P297, DOI 10.1056/NEJM199302043280501
  32. National Research Council, 1996, GUID CAR US LAB AN P
  33. Nieto A, 2011, VET RES, V42, DOI 10.1186/1297-9716-42-39
  34. Oliveira Janaina Michelle de, 2010, Rev Soc Bras Med Trop, V43, P188, DOI 10.1590/S0037-86822010000200016
  35. OTT KJ, 1967, J PARASITOL, V53, P641, DOI 10.2307/3276733
  36. PAGANELLI R, 1981, CLIN EXP IMMUNOL, V46, P44
  37. Palatnik-de-Sousa CB, 2011, PARASITE VECTOR, V4, DOI 10.1186/1756-3305-4-197
  38. Pedras MJ, 2008, T ROY SOC TROP MED H, V102, P172, DOI 10.1016/j.trstmh.2007.11.004
  39. Porrozzi R, 2007, CLIN VACCINE IMMUNOL, V14, P544, DOI 10.1128/CVI.00420-06
  40. Romero HD, 2009, AM J TROP MED HYG, V81, P27
  41. Senaldi G, 1996, J IMMUNOL METHODS, V193, P9, DOI 10.1016/0022-1759(96)00037-3
  42. Singh RK, 2006, INDIAN J MED RES, V123, P331
  43. Singh S, 2006, INDIAN J MED RES, V123, P311
  44. Soares NM, 2001, J IMMUNOL METHODS, V249, P199, DOI 10.1016/S0022-1759(00)00362-8
  45. Solano-Gallego L, 2009, VET PARASITOL, V165, P1, DOI 10.1016/j.vetpar.2009.05.022
  46. Srivastava P, 2011, T ROY SOC TROP MED H, V105, P1, DOI 10.1016/j.trstmh.2010.09.006
  47. Stanley AC, 2007, IMMUNOL CELL BIOL, V85, P138, DOI 10.1038/sj.icb.7100011
  48. Swartzentruber S, 2009, CLIN VACCINE IMMUNOL, V16, P320, DOI 10.1128/CVI.00409-08
  49. VINAYAK VK, 1986, J CLIN MICROBIOL, V23, P1088
  50. Werneck GL, 2007, EPIDEMIOL INFECT, V135, P195, DOI 10.1017/S095026806006881
  51. WHO, 2012, RES TRAIN TROP DIS N