Investigation of residual hepatitis C virus in presumed recovered subjects

Autores
Fujiwara, Kei; Allison, Robert. D.; Wang, Richard Y.; Baré, Patricia; Matsuura, Kentaro; Schechterly, Cathy; Murthy, Krishna; Marincola, Francesco M.; Alter, Harvey J.
Año de publicación
2013
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Recent studies have found hepatitis C virus (HCV) RNA in peripheral blood mononuclear cells (PBMCs) of the majority of presumed recovered subjects. We investigated this unexpected finding using samples from patients whose HCV RNA and anti-HCV status had been serially confirmed. HCV RNA was detected in PBMCs from 66/67 chronic HCV carriers. Subpopulation analysis revealed that the viral load (log copies/10(6) cells) in B cells (4.14 ± 0.71) was higher than in total PBMCs (3.62 ± 0.71, p<0.05), T cells (1.67 ± 0.88, p<0.05), and non-B/T cells (2.48 ± 1.15, p<0.05). HCV negative-strand RNA was not detected in PBMCs from any of 25 chronically infected patients. No residual viral RNA was detected in total PBMCs or plasma of 59 presumed recovered subjects (11 spontaneous, 48 treatment-induced) using nested real-time PCR with a detection limit of 2 copies/µg RNA (from ∼1x10(6) cells). PBMCs from two healthy HCV-negative blood donors became HCV RNA positive, with B-cell predominance, when mixed in vitro with HCV RNA positive plasma, thus passively mimicking cells from chronic HCV carriers. No residual HCV was detected in liver or other tissues from two spontaneously recovered chimpanzees. Conclusion: 1) HCV RNA was detected in PBMCs of most chronic HCV carriers and was predominant in the B cell subpopulation; 2) HCV detected in PBMCs was in a non-replicative form; 3) HCV passively adsorbed to PBMCs of healthy controls in vitro becoming indistinguishable from PBMCs of chronic HCV carriers; 4) Residual HCV was not detected in the plasma or PBMCs of any spontaneous or treatment recovered subjects or in chimpanzee liver suggesting that the classic pattern of recovery from HCV infection is generally equivalent to viral eradication.
Fil: Fujiwara, Kei. National Institutes of Health; Estados Unidos
Fil: Allison, Robert. D.. National Institutes of Health; Estados Unidos. United States Navy; Estados Unidos
Fil: Wang, Richard Y.. National Institutes of Health; Estados Unidos
Fil: Baré, Patricia. National Institutes of Health; Estados Unidos. Academia Nacional de Medicina de Buenos Aires; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Matsuura, Kentaro. Nagoya City University; Japón
Fil: Schechterly, Cathy. National Institutes of Health; Estados Unidos
Fil: Murthy, Krishna.
Fil: Marincola, Francesco M.. National Institutes of Health; Estados Unidos
Fil: Alter, Harvey J.. National Institutes of Health; Estados Unidos
Materia
Hcv
Residual
Recovery
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/20790

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network_acronym_str CONICETDig
repository_id_str 3498
network_name_str CONICET Digital (CONICET)
spelling Investigation of residual hepatitis C virus in presumed recovered subjectsFujiwara, KeiAllison, Robert. D.Wang, Richard Y.Baré, PatriciaMatsuura, KentaroSchechterly, CathyMurthy, KrishnaMarincola, Francesco M.Alter, Harvey J.HcvResidualRecoveryhttps://purl.org/becyt/ford/3.3https://purl.org/becyt/ford/3Recent studies have found hepatitis C virus (HCV) RNA in peripheral blood mononuclear cells (PBMCs) of the majority of presumed recovered subjects. We investigated this unexpected finding using samples from patients whose HCV RNA and anti-HCV status had been serially confirmed. HCV RNA was detected in PBMCs from 66/67 chronic HCV carriers. Subpopulation analysis revealed that the viral load (log copies/10(6) cells) in B cells (4.14 ± 0.71) was higher than in total PBMCs (3.62 ± 0.71, p<0.05), T cells (1.67 ± 0.88, p<0.05), and non-B/T cells (2.48 ± 1.15, p<0.05). HCV negative-strand RNA was not detected in PBMCs from any of 25 chronically infected patients. No residual viral RNA was detected in total PBMCs or plasma of 59 presumed recovered subjects (11 spontaneous, 48 treatment-induced) using nested real-time PCR with a detection limit of 2 copies/µg RNA (from ∼1x10(6) cells). PBMCs from two healthy HCV-negative blood donors became HCV RNA positive, with B-cell predominance, when mixed in vitro with HCV RNA positive plasma, thus passively mimicking cells from chronic HCV carriers. No residual HCV was detected in liver or other tissues from two spontaneously recovered chimpanzees. Conclusion: 1) HCV RNA was detected in PBMCs of most chronic HCV carriers and was predominant in the B cell subpopulation; 2) HCV detected in PBMCs was in a non-replicative form; 3) HCV passively adsorbed to PBMCs of healthy controls in vitro becoming indistinguishable from PBMCs of chronic HCV carriers; 4) Residual HCV was not detected in the plasma or PBMCs of any spontaneous or treatment recovered subjects or in chimpanzee liver suggesting that the classic pattern of recovery from HCV infection is generally equivalent to viral eradication.Fil: Fujiwara, Kei. National Institutes of Health; Estados UnidosFil: Allison, Robert. D.. National Institutes of Health; Estados Unidos. United States Navy; Estados UnidosFil: Wang, Richard Y.. National Institutes of Health; Estados UnidosFil: Baré, Patricia. National Institutes of Health; Estados Unidos. Academia Nacional de Medicina de Buenos Aires; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Matsuura, Kentaro. Nagoya City University; JapónFil: Schechterly, Cathy. National Institutes of Health; Estados UnidosFil: Murthy, Krishna.Fil: Marincola, Francesco M.. National Institutes of Health; Estados UnidosFil: Alter, Harvey J.. National Institutes of Health; Estados UnidosWiley2013-02info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/vnd.openxmlformats-officedocument.wordprocessingml.documentapplication/pdfhttp://hdl.handle.net/11336/20790Fujiwara, Kei; Allison, Robert. D.; Wang, Richard Y.; Baré, Patricia; Matsuura, Kentaro; et al.; Investigation of residual hepatitis C virus in presumed recovered subjects; Wiley; Hepatology (baltimore, Md.); 57; 2; 2-2013; 483-4910270-91391527-3350CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/http://onlinelibrary.wiley.com/doi/10.1002/hep.25921/abstractinfo:eu-repo/semantics/altIdentifier/doi/10.1002/hep.25921info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-10-22T11:46:52Zoai:ri.conicet.gov.ar:11336/20790instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-10-22 11:46:52.67CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Investigation of residual hepatitis C virus in presumed recovered subjects
title Investigation of residual hepatitis C virus in presumed recovered subjects
spellingShingle Investigation of residual hepatitis C virus in presumed recovered subjects
Fujiwara, Kei
Hcv
Residual
Recovery
title_short Investigation of residual hepatitis C virus in presumed recovered subjects
title_full Investigation of residual hepatitis C virus in presumed recovered subjects
title_fullStr Investigation of residual hepatitis C virus in presumed recovered subjects
title_full_unstemmed Investigation of residual hepatitis C virus in presumed recovered subjects
title_sort Investigation of residual hepatitis C virus in presumed recovered subjects
dc.creator.none.fl_str_mv Fujiwara, Kei
Allison, Robert. D.
Wang, Richard Y.
Baré, Patricia
Matsuura, Kentaro
Schechterly, Cathy
Murthy, Krishna
Marincola, Francesco M.
Alter, Harvey J.
author Fujiwara, Kei
author_facet Fujiwara, Kei
Allison, Robert. D.
Wang, Richard Y.
Baré, Patricia
Matsuura, Kentaro
Schechterly, Cathy
Murthy, Krishna
Marincola, Francesco M.
Alter, Harvey J.
author_role author
author2 Allison, Robert. D.
Wang, Richard Y.
Baré, Patricia
Matsuura, Kentaro
Schechterly, Cathy
Murthy, Krishna
Marincola, Francesco M.
Alter, Harvey J.
author2_role author
author
author
author
author
author
author
author
dc.subject.none.fl_str_mv Hcv
Residual
Recovery
topic Hcv
Residual
Recovery
purl_subject.fl_str_mv https://purl.org/becyt/ford/3.3
https://purl.org/becyt/ford/3
dc.description.none.fl_txt_mv Recent studies have found hepatitis C virus (HCV) RNA in peripheral blood mononuclear cells (PBMCs) of the majority of presumed recovered subjects. We investigated this unexpected finding using samples from patients whose HCV RNA and anti-HCV status had been serially confirmed. HCV RNA was detected in PBMCs from 66/67 chronic HCV carriers. Subpopulation analysis revealed that the viral load (log copies/10(6) cells) in B cells (4.14 ± 0.71) was higher than in total PBMCs (3.62 ± 0.71, p<0.05), T cells (1.67 ± 0.88, p<0.05), and non-B/T cells (2.48 ± 1.15, p<0.05). HCV negative-strand RNA was not detected in PBMCs from any of 25 chronically infected patients. No residual viral RNA was detected in total PBMCs or plasma of 59 presumed recovered subjects (11 spontaneous, 48 treatment-induced) using nested real-time PCR with a detection limit of 2 copies/µg RNA (from ∼1x10(6) cells). PBMCs from two healthy HCV-negative blood donors became HCV RNA positive, with B-cell predominance, when mixed in vitro with HCV RNA positive plasma, thus passively mimicking cells from chronic HCV carriers. No residual HCV was detected in liver or other tissues from two spontaneously recovered chimpanzees. Conclusion: 1) HCV RNA was detected in PBMCs of most chronic HCV carriers and was predominant in the B cell subpopulation; 2) HCV detected in PBMCs was in a non-replicative form; 3) HCV passively adsorbed to PBMCs of healthy controls in vitro becoming indistinguishable from PBMCs of chronic HCV carriers; 4) Residual HCV was not detected in the plasma or PBMCs of any spontaneous or treatment recovered subjects or in chimpanzee liver suggesting that the classic pattern of recovery from HCV infection is generally equivalent to viral eradication.
Fil: Fujiwara, Kei. National Institutes of Health; Estados Unidos
Fil: Allison, Robert. D.. National Institutes of Health; Estados Unidos. United States Navy; Estados Unidos
Fil: Wang, Richard Y.. National Institutes of Health; Estados Unidos
Fil: Baré, Patricia. National Institutes of Health; Estados Unidos. Academia Nacional de Medicina de Buenos Aires; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Matsuura, Kentaro. Nagoya City University; Japón
Fil: Schechterly, Cathy. National Institutes of Health; Estados Unidos
Fil: Murthy, Krishna.
Fil: Marincola, Francesco M.. National Institutes of Health; Estados Unidos
Fil: Alter, Harvey J.. National Institutes of Health; Estados Unidos
description Recent studies have found hepatitis C virus (HCV) RNA in peripheral blood mononuclear cells (PBMCs) of the majority of presumed recovered subjects. We investigated this unexpected finding using samples from patients whose HCV RNA and anti-HCV status had been serially confirmed. HCV RNA was detected in PBMCs from 66/67 chronic HCV carriers. Subpopulation analysis revealed that the viral load (log copies/10(6) cells) in B cells (4.14 ± 0.71) was higher than in total PBMCs (3.62 ± 0.71, p<0.05), T cells (1.67 ± 0.88, p<0.05), and non-B/T cells (2.48 ± 1.15, p<0.05). HCV negative-strand RNA was not detected in PBMCs from any of 25 chronically infected patients. No residual viral RNA was detected in total PBMCs or plasma of 59 presumed recovered subjects (11 spontaneous, 48 treatment-induced) using nested real-time PCR with a detection limit of 2 copies/µg RNA (from ∼1x10(6) cells). PBMCs from two healthy HCV-negative blood donors became HCV RNA positive, with B-cell predominance, when mixed in vitro with HCV RNA positive plasma, thus passively mimicking cells from chronic HCV carriers. No residual HCV was detected in liver or other tissues from two spontaneously recovered chimpanzees. Conclusion: 1) HCV RNA was detected in PBMCs of most chronic HCV carriers and was predominant in the B cell subpopulation; 2) HCV detected in PBMCs was in a non-replicative form; 3) HCV passively adsorbed to PBMCs of healthy controls in vitro becoming indistinguishable from PBMCs of chronic HCV carriers; 4) Residual HCV was not detected in the plasma or PBMCs of any spontaneous or treatment recovered subjects or in chimpanzee liver suggesting that the classic pattern of recovery from HCV infection is generally equivalent to viral eradication.
publishDate 2013
dc.date.none.fl_str_mv 2013-02
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/20790
Fujiwara, Kei; Allison, Robert. D.; Wang, Richard Y.; Baré, Patricia; Matsuura, Kentaro; et al.; Investigation of residual hepatitis C virus in presumed recovered subjects; Wiley; Hepatology (baltimore, Md.); 57; 2; 2-2013; 483-491
0270-9139
1527-3350
CONICET Digital
CONICET
url http://hdl.handle.net/11336/20790
identifier_str_mv Fujiwara, Kei; Allison, Robert. D.; Wang, Richard Y.; Baré, Patricia; Matsuura, Kentaro; et al.; Investigation of residual hepatitis C virus in presumed recovered subjects; Wiley; Hepatology (baltimore, Md.); 57; 2; 2-2013; 483-491
0270-9139
1527-3350
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/http://onlinelibrary.wiley.com/doi/10.1002/hep.25921/abstract
info:eu-repo/semantics/altIdentifier/doi/10.1002/hep.25921
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
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dc.publisher.none.fl_str_mv Wiley
publisher.none.fl_str_mv Wiley
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reponame_str CONICET Digital (CONICET)
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