Serodiagnosis of Leishmania donovani infections: assessment of enzyme-linked immunosorbent assays using recombinant L. donovani gene B protein (GBP) and a peptide sequence of L. donovani GBP

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Standard

Serodiagnosis of Leishmania donovani infections: assessment of enzyme-linked immunosorbent assays using recombinant L. donovani gene B protein (GBP) and a peptide sequence of L. donovani GBP. / Jensen, A T; Gasim, S; Moller, T; Ismail, A; Gaafar, A; Kemp, M; el Hassan, A M; Kharazmi, A; Alce, T M; Smith, D F; Theander, T G.

I: Transactions of the Royal Society of Tropical Medicine and Hygiene, Bind 93, Nr. 2, 1999, s. 157-60.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Jensen, AT, Gasim, S, Moller, T, Ismail, A, Gaafar, A, Kemp, M, el Hassan, AM, Kharazmi, A, Alce, TM, Smith, DF & Theander, TG 1999, 'Serodiagnosis of Leishmania donovani infections: assessment of enzyme-linked immunosorbent assays using recombinant L. donovani gene B protein (GBP) and a peptide sequence of L. donovani GBP', Transactions of the Royal Society of Tropical Medicine and Hygiene, bind 93, nr. 2, s. 157-60.

APA

Jensen, A. T., Gasim, S., Moller, T., Ismail, A., Gaafar, A., Kemp, M., el Hassan, A. M., Kharazmi, A., Alce, T. M., Smith, D. F., & Theander, T. G. (1999). Serodiagnosis of Leishmania donovani infections: assessment of enzyme-linked immunosorbent assays using recombinant L. donovani gene B protein (GBP) and a peptide sequence of L. donovani GBP. Transactions of the Royal Society of Tropical Medicine and Hygiene, 93(2), 157-60.

Vancouver

Jensen AT, Gasim S, Moller T, Ismail A, Gaafar A, Kemp M o.a. Serodiagnosis of Leishmania donovani infections: assessment of enzyme-linked immunosorbent assays using recombinant L. donovani gene B protein (GBP) and a peptide sequence of L. donovani GBP. Transactions of the Royal Society of Tropical Medicine and Hygiene. 1999;93(2):157-60.

Author

Jensen, A T ; Gasim, S ; Moller, T ; Ismail, A ; Gaafar, A ; Kemp, M ; el Hassan, A M ; Kharazmi, A ; Alce, T M ; Smith, D F ; Theander, T G. / Serodiagnosis of Leishmania donovani infections: assessment of enzyme-linked immunosorbent assays using recombinant L. donovani gene B protein (GBP) and a peptide sequence of L. donovani GBP. I: Transactions of the Royal Society of Tropical Medicine and Hygiene. 1999 ; Bind 93, Nr. 2. s. 157-60.

Bibtex

@article{d0e479b0a0d711dd86a6000ea68e967b,
title = "Serodiagnosis of Leishmania donovani infections: assessment of enzyme-linked immunosorbent assays using recombinant L. donovani gene B protein (GBP) and a peptide sequence of L. donovani GBP",
abstract = "The repetitive sequence of Leishmania major gene B protein (GBP) has previously been shown to be a useful tool in the diagnosis of cutaneous leishmaniasis (CL). Here, we have assessed enzyme-linked immunosorbent assays (ELISAs) using recombinant L. donovani GBP (rGBP) and a peptide sequence of L. donovani GBP (GBPP) in the diagnosis of L. donovani infections in Sudan. The sensitivity of the rGBP ELISA in diagnosing visceral leishmaniasis (VL) and post kala-azar dermal leishmaniasis (PKDL) was 92% and 93%, respectively. In contrast, the sensitivity of the GBPP ELISA was 55% for VL and 63% for PKDL. Plasma antibody reactivity of donors with VL and PKDL remained high for an extended period after the end of treatment. Antibody-reactivity to rGBP and GBPP was detected in 71% and 14% of plasma samples from CL patients, respectively. Plasma from healthy Sudanese donors living in an area endemic for malaria but free of leishmaniasis was negative in both assays.",
author = "Jensen, {A T} and S Gasim and T Moller and A Ismail and A Gaafar and M Kemp and {el Hassan}, {A M} and A Kharazmi and Alce, {T M} and Smith, {D F} and Theander, {T G}",
note = "Keywords: Adolescent; Adult; Animals; Child; Enzyme-Linked Immunosorbent Assay; Female; Humans; Immunoglobulin G; Leishmania donovani; Leishmaniasis, Cutaneous; Leishmaniasis, Visceral; Male; Middle Aged; Protozoan Proteins; Recombinant Proteins; Repetitive Sequences, Amino Acid; Sensitivity and Specificity",
year = "1999",
language = "English",
volume = "93",
pages = "157--60",
journal = "Transactions of the Royal Society of Tropical Medicine and Hygiene",
issn = "0035-9203",
publisher = "Oxford University Press",
number = "2",

}

RIS

TY - JOUR

T1 - Serodiagnosis of Leishmania donovani infections: assessment of enzyme-linked immunosorbent assays using recombinant L. donovani gene B protein (GBP) and a peptide sequence of L. donovani GBP

AU - Jensen, A T

AU - Gasim, S

AU - Moller, T

AU - Ismail, A

AU - Gaafar, A

AU - Kemp, M

AU - el Hassan, A M

AU - Kharazmi, A

AU - Alce, T M

AU - Smith, D F

AU - Theander, T G

N1 - Keywords: Adolescent; Adult; Animals; Child; Enzyme-Linked Immunosorbent Assay; Female; Humans; Immunoglobulin G; Leishmania donovani; Leishmaniasis, Cutaneous; Leishmaniasis, Visceral; Male; Middle Aged; Protozoan Proteins; Recombinant Proteins; Repetitive Sequences, Amino Acid; Sensitivity and Specificity

PY - 1999

Y1 - 1999

N2 - The repetitive sequence of Leishmania major gene B protein (GBP) has previously been shown to be a useful tool in the diagnosis of cutaneous leishmaniasis (CL). Here, we have assessed enzyme-linked immunosorbent assays (ELISAs) using recombinant L. donovani GBP (rGBP) and a peptide sequence of L. donovani GBP (GBPP) in the diagnosis of L. donovani infections in Sudan. The sensitivity of the rGBP ELISA in diagnosing visceral leishmaniasis (VL) and post kala-azar dermal leishmaniasis (PKDL) was 92% and 93%, respectively. In contrast, the sensitivity of the GBPP ELISA was 55% for VL and 63% for PKDL. Plasma antibody reactivity of donors with VL and PKDL remained high for an extended period after the end of treatment. Antibody-reactivity to rGBP and GBPP was detected in 71% and 14% of plasma samples from CL patients, respectively. Plasma from healthy Sudanese donors living in an area endemic for malaria but free of leishmaniasis was negative in both assays.

AB - The repetitive sequence of Leishmania major gene B protein (GBP) has previously been shown to be a useful tool in the diagnosis of cutaneous leishmaniasis (CL). Here, we have assessed enzyme-linked immunosorbent assays (ELISAs) using recombinant L. donovani GBP (rGBP) and a peptide sequence of L. donovani GBP (GBPP) in the diagnosis of L. donovani infections in Sudan. The sensitivity of the rGBP ELISA in diagnosing visceral leishmaniasis (VL) and post kala-azar dermal leishmaniasis (PKDL) was 92% and 93%, respectively. In contrast, the sensitivity of the GBPP ELISA was 55% for VL and 63% for PKDL. Plasma antibody reactivity of donors with VL and PKDL remained high for an extended period after the end of treatment. Antibody-reactivity to rGBP and GBPP was detected in 71% and 14% of plasma samples from CL patients, respectively. Plasma from healthy Sudanese donors living in an area endemic for malaria but free of leishmaniasis was negative in both assays.

M3 - Journal article

C2 - 10450438

VL - 93

SP - 157

EP - 160

JO - Transactions of the Royal Society of Tropical Medicine and Hygiene

JF - Transactions of the Royal Society of Tropical Medicine and Hygiene

SN - 0035-9203

IS - 2

ER -

ID: 6765867