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Longitudinal alteration of circulating dendritic cell subsets and its correlation with steroid treatment in patients with severe acute respiratory syndrome

Identifieur interne : 000611 ( PascalFrancis/Corpus ); précédent : 000610; suivant : 000612

Longitudinal alteration of circulating dendritic cell subsets and its correlation with steroid treatment in patients with severe acute respiratory syndrome

Auteurs : ZHENG ZHANG ; DONGPING XU ; YONGGANG LI ; LEI JIN ; MING SHI ; MIN WANG ; XIANZHI ZHOU ; HAO WU ; George F. Gao ; Fu-Sheng Wang

Source :

RBID : Pascal:05-0404718

Descripteurs français

English descriptors

Abstract

In this study, we found that 74 patients with severe acute respiratory syndrome (SARS) exhibited a rapid, dramatic decrease in numbers of circulating myeloid and plasmacytoid dendritic cells (mDCs and pDCs) during the first 2 weeks of illness (5.3- and 28.4-fold reductions for mDCs and pDCs compared with 25 healthy individuals, respectively), with slow return to normal cell numbers during convalescence (weeks 5-7 of illness on average). In addition, numbers of circulating CD4 and CD8 T cells exhibited milder reductions (2.1- and 1.8-fold at week 1) and earlier return to normal at a mean of weeks 3 and 4, respectively. A significant inverse correlation was found between numbers of DC and T-cell subsets and high-dose steroid treatment. Our novel findings thus suggest that the acute SARS-coronavirus infection probably contributes to the initial reduction of DC and T-cell subsets in blood, and that high-dose steroid administration may subsequently exacerbate and prolong low expression of the cell subsets. These findings will aid the framing of further studies of the immunopathogenesis of SARS.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

pA  
A01 01  1    @0 1521-6616
A02 01      @0 CLIIFY
A03   1    @0 Clin. immunol. : (Orlando, Fla., Print)
A05       @2 116
A06       @2 3
A08 01  1  ENG  @1 Longitudinal alteration of circulating dendritic cell subsets and its correlation with steroid treatment in patients with severe acute respiratory syndrome
A11 01  1    @1 ZHENG ZHANG
A11 02  1    @1 DONGPING XU
A11 03  1    @1 YONGGANG LI
A11 04  1    @1 LEI JIN
A11 05  1    @1 MING SHI
A11 06  1    @1 MIN WANG
A11 07  1    @1 XIANZHI ZHOU
A11 08  1    @1 HAO WU
A11 09  1    @1 GAO (George F.)
A11 10  1    @1 WANG (Fu-Sheng)
A14 01      @1 Research Centre for Biological Therapy, Beijing Institute of Infectious Diseases, Beijing 302 Hospital, 100 Xi Si Huan Middle Road @2 Beijing 100039 @3 CHN @Z 1 aut. @Z 2 aut. @Z 3 aut. @Z 4 aut. @Z 5 aut. @Z 6 aut. @Z 7 aut. @Z 10 aut.
A14 02      @1 Beijing You'an Hospital, Capital Medical University @2 Beijing 100054 @3 CHN @Z 8 aut.
A14 03      @1 Institute of Microbiology, Chinese Academy of Sciences @2 Beijing 100080 @3 CHN @Z 9 aut.
A20       @1 225-235
A21       @1 2005
A23 01      @0 ENG
A43 01      @1 INIST @2 15461 @5 354000131594300050
A44       @0 0000 @1 © 2005 INIST-CNRS. All rights reserved.
A45       @0 48 ref.
A47 01  1    @0 05-0404718
A60       @1 P
A61       @0 A
A64 01  1    @0 Clinical immunology : (Orlando, Fla. Print)
A66 01      @0 USA
C01 01    ENG  @0 In this study, we found that 74 patients with severe acute respiratory syndrome (SARS) exhibited a rapid, dramatic decrease in numbers of circulating myeloid and plasmacytoid dendritic cells (mDCs and pDCs) during the first 2 weeks of illness (5.3- and 28.4-fold reductions for mDCs and pDCs compared with 25 healthy individuals, respectively), with slow return to normal cell numbers during convalescence (weeks 5-7 of illness on average). In addition, numbers of circulating CD4 and CD8 T cells exhibited milder reductions (2.1- and 1.8-fold at week 1) and earlier return to normal at a mean of weeks 3 and 4, respectively. A significant inverse correlation was found between numbers of DC and T-cell subsets and high-dose steroid treatment. Our novel findings thus suggest that the acute SARS-coronavirus infection probably contributes to the initial reduction of DC and T-cell subsets in blood, and that high-dose steroid administration may subsequently exacerbate and prolong low expression of the cell subsets. These findings will aid the framing of further studies of the immunopathogenesis of SARS.
C02 01  X    @0 002B06
C02 02  X    @0 002A06
C03 01  X  FRE  @0 Syndrome respiratoire aigu sévère @2 NM @5 01
C03 01  X  ENG  @0 Severe acute respiratory syndrome @2 NM @5 01
C03 01  X  SPA  @0 Síndrome respiratorio agudo severo @2 NM @5 01
C03 02  X  FRE  @0 Cellule dendritique @5 02
C03 02  X  ENG  @0 Dendritic cell @5 02
C03 02  X  SPA  @0 Célula dendrítica @5 02
C03 03  X  FRE  @0 Cellule APC @5 03
C03 03  X  ENG  @0 Antigen presenting cell @5 03
C03 03  X  SPA  @0 Célula presentadora de antígeno @5 03
C03 04  X  FRE  @0 Stéroïde @5 05
C03 04  X  ENG  @0 Steroid @5 05
C03 04  X  SPA  @0 Esteroide @5 05
C03 05  X  FRE  @0 Traitement @5 06
C03 05  X  ENG  @0 Treatment @5 06
C03 05  X  SPA  @0 Tratamiento @5 06
C03 06  X  FRE  @0 Homme @5 08
C03 06  X  ENG  @0 Human @5 08
C03 06  X  SPA  @0 Hombre @5 08
C03 07  X  FRE  @0 Coronavirus @2 NW @5 09
C03 07  X  ENG  @0 Coronavirus @2 NW @5 09
C03 07  X  SPA  @0 Coronavirus @2 NW @5 09
C03 08  X  FRE  @0 Cellule dendritique myéloïde @4 CD @5 96
C03 08  X  ENG  @0 Myeloid dendritic cell @4 CD @5 96
C03 09  X  FRE  @0 Cellule dendritique plasmocytoïde @4 CD @5 97
C03 09  X  ENG  @0 Plasmacytoid dendritic cell @4 CD @5 97
C07 01  X  FRE  @0 Virose
C07 01  X  ENG  @0 Viral disease
C07 01  X  SPA  @0 Virosis
C07 02  X  FRE  @0 Infection
C07 02  X  ENG  @0 Infection
C07 02  X  SPA  @0 Infección
C07 03  X  FRE  @0 Coronaviridae @2 NW
C07 03  X  ENG  @0 Coronaviridae @2 NW
C07 03  X  SPA  @0 Coronaviridae @2 NW
C07 04  X  FRE  @0 Nidovirales @2 NW
C07 04  X  ENG  @0 Nidovirales @2 NW
C07 04  X  SPA  @0 Nidovirales @2 NW
C07 05  X  FRE  @0 Virus @2 NW
C07 05  X  ENG  @0 Virus @2 NW
C07 05  X  SPA  @0 Virus @2 NW
C07 06  X  FRE  @0 Immunologie @5 37
C07 06  X  ENG  @0 Immunology @5 37
C07 06  X  SPA  @0 Inmunología @5 37
C07 07  X  FRE  @0 Immunopathologie @5 38
C07 07  X  ENG  @0 Immunopathology @5 38
C07 07  X  SPA  @0 Inmunopatología @5 38
C07 08  X  FRE  @0 Appareil respiratoire pathologie @5 39
C07 08  X  ENG  @0 Respiratory disease @5 39
C07 08  X  SPA  @0 Aparato respiratorio patología @5 39
C07 09  X  FRE  @0 Poumon pathologie @5 40
C07 09  X  ENG  @0 Lung disease @5 40
C07 09  X  SPA  @0 Pulmón patología @5 40
N21       @1 283
N44 01      @1 OTO
N82       @1 OTO

Format Inist (serveur)

NO : PASCAL 05-0404718 INIST
ET : Longitudinal alteration of circulating dendritic cell subsets and its correlation with steroid treatment in patients with severe acute respiratory syndrome
AU : ZHENG ZHANG; DONGPING XU; YONGGANG LI; LEI JIN; MING SHI; MIN WANG; XIANZHI ZHOU; HAO WU; GAO (George F.); WANG (Fu-Sheng)
AF : Research Centre for Biological Therapy, Beijing Institute of Infectious Diseases, Beijing 302 Hospital, 100 Xi Si Huan Middle Road/Beijing 100039/Chine (1 aut., 2 aut., 3 aut., 4 aut., 5 aut., 6 aut., 7 aut., 10 aut.); Beijing You'an Hospital, Capital Medical University/Beijing 100054/Chine (8 aut.); Institute of Microbiology, Chinese Academy of Sciences/Beijing 100080/Chine (9 aut.)
DT : Publication en série; Niveau analytique
SO : Clinical immunology : (Orlando, Fla. Print); ISSN 1521-6616; Coden CLIIFY; Etats-Unis; Da. 2005; Vol. 116; No. 3; Pp. 225-235; Bibl. 48 ref.
LA : Anglais
EA : In this study, we found that 74 patients with severe acute respiratory syndrome (SARS) exhibited a rapid, dramatic decrease in numbers of circulating myeloid and plasmacytoid dendritic cells (mDCs and pDCs) during the first 2 weeks of illness (5.3- and 28.4-fold reductions for mDCs and pDCs compared with 25 healthy individuals, respectively), with slow return to normal cell numbers during convalescence (weeks 5-7 of illness on average). In addition, numbers of circulating CD4 and CD8 T cells exhibited milder reductions (2.1- and 1.8-fold at week 1) and earlier return to normal at a mean of weeks 3 and 4, respectively. A significant inverse correlation was found between numbers of DC and T-cell subsets and high-dose steroid treatment. Our novel findings thus suggest that the acute SARS-coronavirus infection probably contributes to the initial reduction of DC and T-cell subsets in blood, and that high-dose steroid administration may subsequently exacerbate and prolong low expression of the cell subsets. These findings will aid the framing of further studies of the immunopathogenesis of SARS.
CC : 002B06; 002A06
FD : Syndrome respiratoire aigu sévère; Cellule dendritique; Cellule APC; Stéroïde; Traitement; Homme; Coronavirus; Cellule dendritique myéloïde; Cellule dendritique plasmocytoïde
FG : Virose; Infection; Coronaviridae; Nidovirales; Virus; Immunologie; Immunopathologie; Appareil respiratoire pathologie; Poumon pathologie
ED : Severe acute respiratory syndrome; Dendritic cell; Antigen presenting cell; Steroid; Treatment; Human; Coronavirus; Myeloid dendritic cell; Plasmacytoid dendritic cell
EG : Viral disease; Infection; Coronaviridae; Nidovirales; Virus; Immunology; Immunopathology; Respiratory disease; Lung disease
SD : Síndrome respiratorio agudo severo; Célula dendrítica; Célula presentadora de antígeno; Esteroide; Tratamiento; Hombre; Coronavirus
LO : INIST-15461.354000131594300050
ID : 05-0404718

Links to Exploration step

Pascal:05-0404718

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<div type="abstract" xml:lang="en">In this study, we found that 74 patients with severe acute respiratory syndrome (SARS) exhibited a rapid, dramatic decrease in numbers of circulating myeloid and plasmacytoid dendritic cells (mDCs and pDCs) during the first 2 weeks of illness (5.3- and 28.4-fold reductions for mDCs and pDCs compared with 25 healthy individuals, respectively), with slow return to normal cell numbers during convalescence (weeks 5-7 of illness on average). In addition, numbers of circulating CD4 and CD8 T cells exhibited milder reductions (2.1- and 1.8-fold at week 1) and earlier return to normal at a mean of weeks 3 and 4, respectively. A significant inverse correlation was found between numbers of DC and T-cell subsets and high-dose steroid treatment. Our novel findings thus suggest that the acute SARS-coronavirus infection probably contributes to the initial reduction of DC and T-cell subsets in blood, and that high-dose steroid administration may subsequently exacerbate and prolong low expression of the cell subsets. These findings will aid the framing of further studies of the immunopathogenesis of SARS.</div>
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<ET>Longitudinal alteration of circulating dendritic cell subsets and its correlation with steroid treatment in patients with severe acute respiratory syndrome</ET>
<AU>ZHENG ZHANG; DONGPING XU; YONGGANG LI; LEI JIN; MING SHI; MIN WANG; XIANZHI ZHOU; HAO WU; GAO (George F.); WANG (Fu-Sheng)</AU>
<AF>Research Centre for Biological Therapy, Beijing Institute of Infectious Diseases, Beijing 302 Hospital, 100 Xi Si Huan Middle Road/Beijing 100039/Chine (1 aut., 2 aut., 3 aut., 4 aut., 5 aut., 6 aut., 7 aut., 10 aut.); Beijing You'an Hospital, Capital Medical University/Beijing 100054/Chine (8 aut.); Institute of Microbiology, Chinese Academy of Sciences/Beijing 100080/Chine (9 aut.)</AF>
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<EA>In this study, we found that 74 patients with severe acute respiratory syndrome (SARS) exhibited a rapid, dramatic decrease in numbers of circulating myeloid and plasmacytoid dendritic cells (mDCs and pDCs) during the first 2 weeks of illness (5.3- and 28.4-fold reductions for mDCs and pDCs compared with 25 healthy individuals, respectively), with slow return to normal cell numbers during convalescence (weeks 5-7 of illness on average). In addition, numbers of circulating CD4 and CD8 T cells exhibited milder reductions (2.1- and 1.8-fold at week 1) and earlier return to normal at a mean of weeks 3 and 4, respectively. A significant inverse correlation was found between numbers of DC and T-cell subsets and high-dose steroid treatment. Our novel findings thus suggest that the acute SARS-coronavirus infection probably contributes to the initial reduction of DC and T-cell subsets in blood, and that high-dose steroid administration may subsequently exacerbate and prolong low expression of the cell subsets. These findings will aid the framing of further studies of the immunopathogenesis of SARS.</EA>
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