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
.jpg)
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/20790
Ver los metadatos del registro completo
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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. |
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2013 |
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2013-02 |
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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 |
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http://hdl.handle.net/11336/20790 |
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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 |
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eng |
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