Serodiagnosis of cutaneous leishmaniasis: assessment of an enzyme-linked immunosorbent assay using a peptide sequence from gene B protein

A T Jensen; A Gaafar; A Ismail; C B Christensen; M Kemp; A M Hassan; A Kharazmi; T G Theander

Serodiagnosis of cutaneous leishmaniasis: assessment of an enzyme-linked immunosorbent assay using a peptide sequence from gene B protein

A T Jensen, A Gaafar, A Ismail, C B Christensen, M Kemp, A M Hassan, A Kharazmi, T G Theander

Centre for Medical Parasitology

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

29 Citationer (Scopus)

Abstract

Udgivelsesdato: 1996-Nov

Originalsprog	Engelsk
Tidsskrift	American Journal of Tropical Medicine and Hygiene
Vol/bind	55
Udgave nummer	5
Sider (fra-til)	490-5
Antal sider	5
ISSN	0002-9637
Status	Udgivet - 1996

Bibliografisk note

Keywords: Adolescent; Adult; Amino Acid Sequence; Animals; Antibodies, Protozoan; Antigens, Protozoan; Enzyme-Linked Immunosorbent Assay; Female; Humans; Leishmania donovani; Leishmania major; Leishmaniasis, Cutaneous; Male; Metalloendopeptidases; Middle Aged; Molecular Sequence Data; Peptides; Protozoan Proteins; Sensitivity and Specificity; Serologic Tests

Citationsformater

Serodiagnosis of cutaneous leishmaniasis: assessment of an enzyme-linked immunosorbent assay using a peptide sequence from gene B protein. / Jensen, A T; Gaafar, A; Ismail, A; Christensen, C B; Kemp, M; Hassan, A M; Kharazmi, A; Theander, T G.

I: American Journal of Tropical Medicine and Hygiene, Bind 55, Nr. 5, 1996, s. 490-5.

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

@article{82773220a0d911dd86a6000ea68e967b,

title = "Serodiagnosis of cutaneous leishmaniasis: assessment of an enzyme-linked immunosorbent assay using a peptide sequence from gene B protein",

abstract = "An enzyme-linked immunosorbent assay (ELISA) using a 28 amino acid sequence of the repetitive element of gene B protein (GBP) from Leishmania major was developed for serodiagnosis of cutaneous leishmaniasis (CL). The assay was compared to ELISAs using crude amastigote and promastigote antigens from L. donovani and the major surface glycoprotein (Gp63) from either L. donovani or L. major as a solid-phase ligand. The sensitivity of the assays was tested in 33 patients suffering from CL caused by L. major. The sensitivity of the GBP peptide (GBPP) ELISA was 82%. This was higher than in the assays using crude amastigote (67%) or promastigote (67%) antigens, but the difference was not statistically significant. The sensitivity in the assays using Gp63 from L. donovani (52%) or L. major (39%) was significantly lower than in the assay using GBPP (P = 0.019 and P < 0.001, respectively). Plasma samples from healthy Sudanese individuals living in an area endemic for malaria but free of leish-maniasis were negative in all the assays. Significantly higher levels of antibodies were found in the patients who had suffered from the disease for more than eight weeks than in patients with a shorter clinical history (GBPP ELISA; P = 0.038; amastigote ELISA; P = 0.004; and promastigote ELISA; P = 0.017). In the former group, the sensitivities of the five ELISAs were 100% (GBPP), 87% (amastigote), 93% (promastigote), 67% (L. donovani), and 53% (L. major), respectively.",

author = "Jensen, {A T} and A Gaafar and A Ismail and Christensen, {C B} and M Kemp and Hassan, {A M} and A Kharazmi and Theander, {T G}",

note = "Keywords: Adolescent; Adult; Amino Acid Sequence; Animals; Antibodies, Protozoan; Antigens, Protozoan; Enzyme-Linked Immunosorbent Assay; Female; Humans; Leishmania donovani; Leishmania major; Leishmaniasis, Cutaneous; Male; Metalloendopeptidases; Middle Aged; Molecular Sequence Data; Peptides; Protozoan Proteins; Sensitivity and Specificity; Serologic Tests",

year = "1996",

language = "English",

volume = "55",

pages = "490--5",

journal = "Journal. National Malaria Society",

issn = "0002-9637",

publisher = "American Society of Tropical Medicine and Hygiene",

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TY - JOUR

T1 - Serodiagnosis of cutaneous leishmaniasis: assessment of an enzyme-linked immunosorbent assay using a peptide sequence from gene B protein

AU - Jensen, A T

AU - Gaafar, A

AU - Ismail, A

AU - Christensen, C B

AU - Kemp, M

AU - Hassan, A M

AU - Kharazmi, A

AU - Theander, T G

N1 - Keywords: Adolescent; Adult; Amino Acid Sequence; Animals; Antibodies, Protozoan; Antigens, Protozoan; Enzyme-Linked Immunosorbent Assay; Female; Humans; Leishmania donovani; Leishmania major; Leishmaniasis, Cutaneous; Male; Metalloendopeptidases; Middle Aged; Molecular Sequence Data; Peptides; Protozoan Proteins; Sensitivity and Specificity; Serologic Tests

PY - 1996

Y1 - 1996

N2 - An enzyme-linked immunosorbent assay (ELISA) using a 28 amino acid sequence of the repetitive element of gene B protein (GBP) from Leishmania major was developed for serodiagnosis of cutaneous leishmaniasis (CL). The assay was compared to ELISAs using crude amastigote and promastigote antigens from L. donovani and the major surface glycoprotein (Gp63) from either L. donovani or L. major as a solid-phase ligand. The sensitivity of the assays was tested in 33 patients suffering from CL caused by L. major. The sensitivity of the GBP peptide (GBPP) ELISA was 82%. This was higher than in the assays using crude amastigote (67%) or promastigote (67%) antigens, but the difference was not statistically significant. The sensitivity in the assays using Gp63 from L. donovani (52%) or L. major (39%) was significantly lower than in the assay using GBPP (P = 0.019 and P < 0.001, respectively). Plasma samples from healthy Sudanese individuals living in an area endemic for malaria but free of leish-maniasis were negative in all the assays. Significantly higher levels of antibodies were found in the patients who had suffered from the disease for more than eight weeks than in patients with a shorter clinical history (GBPP ELISA; P = 0.038; amastigote ELISA; P = 0.004; and promastigote ELISA; P = 0.017). In the former group, the sensitivities of the five ELISAs were 100% (GBPP), 87% (amastigote), 93% (promastigote), 67% (L. donovani), and 53% (L. major), respectively.

AB - An enzyme-linked immunosorbent assay (ELISA) using a 28 amino acid sequence of the repetitive element of gene B protein (GBP) from Leishmania major was developed for serodiagnosis of cutaneous leishmaniasis (CL). The assay was compared to ELISAs using crude amastigote and promastigote antigens from L. donovani and the major surface glycoprotein (Gp63) from either L. donovani or L. major as a solid-phase ligand. The sensitivity of the assays was tested in 33 patients suffering from CL caused by L. major. The sensitivity of the GBP peptide (GBPP) ELISA was 82%. This was higher than in the assays using crude amastigote (67%) or promastigote (67%) antigens, but the difference was not statistically significant. The sensitivity in the assays using Gp63 from L. donovani (52%) or L. major (39%) was significantly lower than in the assay using GBPP (P = 0.019 and P < 0.001, respectively). Plasma samples from healthy Sudanese individuals living in an area endemic for malaria but free of leish-maniasis were negative in all the assays. Significantly higher levels of antibodies were found in the patients who had suffered from the disease for more than eight weeks than in patients with a shorter clinical history (GBPP ELISA; P = 0.038; amastigote ELISA; P = 0.004; and promastigote ELISA; P = 0.017). In the former group, the sensitivities of the five ELISAs were 100% (GBPP), 87% (amastigote), 93% (promastigote), 67% (L. donovani), and 53% (L. major), respectively.

M3 - Journal article

C2 - 8940979

VL - 55

SP - 490

EP - 495

JO - Journal. National Malaria Society

JF - Journal. National Malaria Society

SN - 0002-9637

IS - 5

ER -