Hepatitis C virus (HCV)-specific immune responses of long-term injection drug users frequently exposed to HCV.

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Hepatitis C virus (HCV)-specific immune responses of long-term injection drug users frequently exposed to HCV. / Mizukoshi, Eishiro; Eisenbach, Christoph; Edlin, Brian R; Newton, Kimberly P; Raghuraman, Sukanya; Weiler-Normann, Christina; Tobler, Leslie H; Busch, Michael P; Carrington, Mary; McKeating, Jane A; O'Brien, Thomas R; Rehermann, Barbara.

in: J INFECT DIS, Jahrgang 198, Nr. 2, 2, 2008, S. 203-212.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Mizukoshi, E, Eisenbach, C, Edlin, BR, Newton, KP, Raghuraman, S, Weiler-Normann, C, Tobler, LH, Busch, MP, Carrington, M, McKeating, JA, O'Brien, TR & Rehermann, B 2008, 'Hepatitis C virus (HCV)-specific immune responses of long-term injection drug users frequently exposed to HCV.', J INFECT DIS, Jg. 198, Nr. 2, 2, S. 203-212. <http://www.ncbi.nlm.nih.gov/pubmed/18505381?dopt=Citation>

APA

Mizukoshi, E., Eisenbach, C., Edlin, B. R., Newton, K. P., Raghuraman, S., Weiler-Normann, C., Tobler, L. H., Busch, M. P., Carrington, M., McKeating, J. A., O'Brien, T. R., & Rehermann, B. (2008). Hepatitis C virus (HCV)-specific immune responses of long-term injection drug users frequently exposed to HCV. J INFECT DIS, 198(2), 203-212. [2]. http://www.ncbi.nlm.nih.gov/pubmed/18505381?dopt=Citation

Vancouver

Mizukoshi E, Eisenbach C, Edlin BR, Newton KP, Raghuraman S, Weiler-Normann C et al. Hepatitis C virus (HCV)-specific immune responses of long-term injection drug users frequently exposed to HCV. J INFECT DIS. 2008;198(2):203-212. 2.

Bibtex

@article{5f30ebee932a42f09fe88c9c59f33944,
title = "Hepatitis C virus (HCV)-specific immune responses of long-term injection drug users frequently exposed to HCV.",
abstract = "BACKGROUND: Injection drug users (IDUs) who successfully clear hepatitis C virus (HCV) have a reduced risk of developing chronic reinfection, despite their continuing exposure to the virus. To identify immunological correlates for this apparent protection, we studied HCV-specific immune responses in long-term IDUs (duration, >10 years). METHODS: HCV-specific T cell responses were assessed in proliferation, enzyme-linked immunospot (ELISPOT), interferon (IFN)-gamma secretion, and cytotoxicity assays, whereas HCV-specific antibodies were assessed in enzyme immunoassays (EIAs), chemiluminescent assays, and in vitro neutralization assays. RESULTS: HCV-specific T cell proliferation and IFN-gamma production were more common in nonviremic EIA-positive IDUs (16 [94%] of 17 IDUs) than in viremic EIA-positive IDUs (9 [45%] of 20 IDUs) (P= .003). They were also noted in 16 (62%) of 26 nonviremic EIA-negative IDUs. In contrast, 19 (90%) of 21 viremic IDUs displayed neutralizing antibodies (nAbs), compared with 9 (56%) of 16 nonviremic EIA-positive IDUs (P= .04) and 0 of 24 nonviremic EIA-negative IDUs. Nonviremic IDUs with nAbs were older (P= .0115) than those without nAbs, but these groups did not differ in terms of either injection drug use duration or HCV-specific T cell responses. CONCLUSION: The reduced risk of HCV persistence in IDUs previously recovered from HCV infection correlated with T cell responses, and prolonged antigenic stimulation appears to be required to maintain humoral responses.",
author = "Eishiro Mizukoshi and Christoph Eisenbach and Edlin, {Brian R} and Newton, {Kimberly P} and Sukanya Raghuraman and Christina Weiler-Normann and Tobler, {Leslie H} and Busch, {Michael P} and Mary Carrington and McKeating, {Jane A} and O'Brien, {Thomas R} and Barbara Rehermann",
year = "2008",
language = "Deutsch",
volume = "198",
pages = "203--212",
journal = "J INFECT DIS",
issn = "0022-1899",
publisher = "Oxford University Press",
number = "2",

}

RIS

TY - JOUR

T1 - Hepatitis C virus (HCV)-specific immune responses of long-term injection drug users frequently exposed to HCV.

AU - Mizukoshi, Eishiro

AU - Eisenbach, Christoph

AU - Edlin, Brian R

AU - Newton, Kimberly P

AU - Raghuraman, Sukanya

AU - Weiler-Normann, Christina

AU - Tobler, Leslie H

AU - Busch, Michael P

AU - Carrington, Mary

AU - McKeating, Jane A

AU - O'Brien, Thomas R

AU - Rehermann, Barbara

PY - 2008

Y1 - 2008

N2 - BACKGROUND: Injection drug users (IDUs) who successfully clear hepatitis C virus (HCV) have a reduced risk of developing chronic reinfection, despite their continuing exposure to the virus. To identify immunological correlates for this apparent protection, we studied HCV-specific immune responses in long-term IDUs (duration, >10 years). METHODS: HCV-specific T cell responses were assessed in proliferation, enzyme-linked immunospot (ELISPOT), interferon (IFN)-gamma secretion, and cytotoxicity assays, whereas HCV-specific antibodies were assessed in enzyme immunoassays (EIAs), chemiluminescent assays, and in vitro neutralization assays. RESULTS: HCV-specific T cell proliferation and IFN-gamma production were more common in nonviremic EIA-positive IDUs (16 [94%] of 17 IDUs) than in viremic EIA-positive IDUs (9 [45%] of 20 IDUs) (P= .003). They were also noted in 16 (62%) of 26 nonviremic EIA-negative IDUs. In contrast, 19 (90%) of 21 viremic IDUs displayed neutralizing antibodies (nAbs), compared with 9 (56%) of 16 nonviremic EIA-positive IDUs (P= .04) and 0 of 24 nonviremic EIA-negative IDUs. Nonviremic IDUs with nAbs were older (P= .0115) than those without nAbs, but these groups did not differ in terms of either injection drug use duration or HCV-specific T cell responses. CONCLUSION: The reduced risk of HCV persistence in IDUs previously recovered from HCV infection correlated with T cell responses, and prolonged antigenic stimulation appears to be required to maintain humoral responses.

AB - BACKGROUND: Injection drug users (IDUs) who successfully clear hepatitis C virus (HCV) have a reduced risk of developing chronic reinfection, despite their continuing exposure to the virus. To identify immunological correlates for this apparent protection, we studied HCV-specific immune responses in long-term IDUs (duration, >10 years). METHODS: HCV-specific T cell responses were assessed in proliferation, enzyme-linked immunospot (ELISPOT), interferon (IFN)-gamma secretion, and cytotoxicity assays, whereas HCV-specific antibodies were assessed in enzyme immunoassays (EIAs), chemiluminescent assays, and in vitro neutralization assays. RESULTS: HCV-specific T cell proliferation and IFN-gamma production were more common in nonviremic EIA-positive IDUs (16 [94%] of 17 IDUs) than in viremic EIA-positive IDUs (9 [45%] of 20 IDUs) (P= .003). They were also noted in 16 (62%) of 26 nonviremic EIA-negative IDUs. In contrast, 19 (90%) of 21 viremic IDUs displayed neutralizing antibodies (nAbs), compared with 9 (56%) of 16 nonviremic EIA-positive IDUs (P= .04) and 0 of 24 nonviremic EIA-negative IDUs. Nonviremic IDUs with nAbs were older (P= .0115) than those without nAbs, but these groups did not differ in terms of either injection drug use duration or HCV-specific T cell responses. CONCLUSION: The reduced risk of HCV persistence in IDUs previously recovered from HCV infection correlated with T cell responses, and prolonged antigenic stimulation appears to be required to maintain humoral responses.

M3 - SCORING: Zeitschriftenaufsatz

VL - 198

SP - 203

EP - 212

JO - J INFECT DIS

JF - J INFECT DIS

SN - 0022-1899

IS - 2

M1 - 2

ER -