493 research outputs found
Direct In Vivo Cell Lineage Analysis in the Retrorsine and 2AAF Models of Liver Injury after Genetic Labeling in Adult and Newborn Rats
- Author
- A Avril
- A Menthena
- AV Kofman
- B Petersen
- BE Petersen
- Christos Samakovlis
- D Aubert
- DH Best
- DH Best
- Dominique Aubert
- E Farber
- GJ Gordon
- GJ Gordon
- GM Higgins
- J Puppi
- K Dezso
- KM Braun
- M Bellodi-Privato
- M Oertel
- M Tatematsu
- MI Yovchev
- MI Yovchev
- MP Bralet
- N Fausto
- Nicolas Ferry
- O Kitten
- P Vig
- R Evarts
- R Kuwahara
- RP Evarts
- S Paku
- SH Oh
- TY Roe
- V Pichard
- V Pichard
- Virginie Pichard
- Publication venue
- Public Library of Science
- Publication date
- 01/09/2009
- Field of study
BACKGROUNDS AND AIMS:When hepatocyte proliferation is impaired, liver regeneration proceeds from the division of non parenchymal hepatocyte progenitors. Oval cells and Small Hepatocyte-like Progenitor Cells (SHPCs) represent the two most studied examples of such epithelial cells with putative stem cell capacity. In the present study we wished to compare the origin of SHPCs proliferating after retrorsine administration to the one of oval cells observed after 2-Acetyl-Amino fluorene (2-AAF) treatment. METHODOLOGY/PRINCIPAL FINDINGS:We used retroviral-mediated nlslacZ genetic labeling of dividing cells to study the fate of cells in the liver. Labeling was performed either in adult rats before treatment or in newborn animals. Labeled cells were identified and characterised by immunohistochemistry. In adult-labeled animals, labeling was restricted to mature hepatocytes. Retrorsine treatment did not modify the overall number of labeled cells in the liver whereas after 2-AAF administration unlabeled oval cells were recorded and the total number of labeled cells decreased significantly. When labeling was performed in newborn rats, results after retrorsine administration were identical to those obtained in adult-labeled rats. In contrast, in the 2-AAF regimen numerous labeled oval cells were present and were able to generate new labeled hepatocytes. Furthermore, we also observed labeled biliary tracts in 2-AAF treated rats. CONCLUSIONS:Our results strongly suggest that SHPCs are derived from hepatocytes and we confirm that SHPCs and oval cells do not share the same origin. We also show that hepatic progenitors are labeled in newborn rats suggesting future directions for in vivo lineage studies
The impact of IL28B genotype on the gene expression profile of patients with chronic hepatitis C treated with pegylated interferon alpha and ribavirin
- Author
- A Birerdinc
- A Mangia
- A Rauch
- AJ Muir
- AJ Thompson
- Ancha Baranova
- Arian Afendy
- Aybike Birerdinc
- B Roe
- C Huang
- C Neumann-Haefelin
- D Ge
- DL Thomas
- E Galmozzi
- G Caignard
- G Indolfi
- H Miyoshi
- H Tang
- HL Tillmann
- J Grebely
- KJ Livak
- M Brysha
- M Honda
- M Lindh
- Maria Stepanova
- Mike Estep
- MJ Alter
- ML Yu
- MP Manns
- MP Martin
- MW Fried
- N Hayashi
- NI Rallon
- P Sharma
- S Brand
- SK Satapathy
- TJ Urban
- TJ Xing
- TY Chen
- V Suppiah
- Z Younossi
- ZM Younossi
- ZM Younossi
- Zobair M Younossi
- Publication venue
- BioMed Central
- Publication date
- 01/01/2012
- Field of study
<p>Abstract</p> <p>Background</p> <p>Recent studies of CH-C patients have demonstrated a strong association between IL28B CC genotype and sustained virologic response (SVR) after PEG-IFN/RBV treatment. We aimed to assess whether IL28B alleles rs12979860 genotype influences gene expression in response to PEG-IFN/RBV in CH-C patients.</p> <p>Methods</p> <p>Clinical data and gene expression data were available for 56 patients treated with PEG-IFN/RBV. Whole blood was used to determine IL28B genotypes. Differential expression of 153 human genes was assessed for each treatment time point (Days: 0, 1, 7, 28, 56) and was correlated with IL28B genotype (IL28B C/C or non-C/C) over the course of the PEG-IFN/RBV treatment. Genes with statistically significant changes in their expression at each time point were used as an input for pathway analysis using KEGG Pathway Painter (KPP). Pathways were ranked based on number of gene involved separately per each study cohort.</p> <p>Results</p> <p>The most striking difference between the response patterns of patients with IL28B C/C and T* genotypes during treatment, across all pathways, is a sustained pattern of treatment-induced gene expression in patients carrying IL28B C/C. In the case of IL28B T* genotype, pre-activation of genes, the lack of sustained pattern of gene expression or a combination of both were observed. This observation could potentially provide an explanation for the lower rate of SVR observed in these patients. Additionally, when the lists of IL28B genotype-specific genes which were differentially expressed in patients without SVR were compared at their baseline, IRF2 and SOCS1 genes were down-regulated regardless of patients' IL28B genotype. Furthermore, our data suggest that CH-C patients who do not have the SOCS1 gene silenced have a better chance of achieving SVR. Our observations suggest that the action of SOCS1 is independent of IL28B genotype.</p> <p>Conclusions</p> <p>IL28B CC genotype patients with CH-C show a sustained treatment-induced gene expression profile which is not seen in non-CC genotype patients. Silencing of SOCS1 is a negative and independent predictor of SVR. These data may provide some mechanistic explanation for higher rate of SVR in IL28B CC patients who are treated with PEG-IFN/RBV.</p
Azimuthal anisotropy of charged particles at high transverse momenta in PbPb collisions at sqrt(s[NN]) = 2.76 TeV
- Author
- Abbaneo D
- Abbiendi G
- Abbrescia M
- Abdullin S
- Abdulsalam A
- Acosta D
- Acosta JG
- Acosta MV
- Adair A
- Adam N
- Adam W
- Adams MR
- Adams T
- Adiguzel A
- Adler V
- Adzic P
- Afanasiev S
- Agostino L
- Agram JL
- Aguilar-Benitez M
- Aguilo E
- Ahmad M
- Ahmad WH
- Ahuja S
- Akchurin N
- Akgun B
- Akgun U
- Akin IV
- Alagoz E
- Albajar C
- Albayrak EA
- Albergo S
- Albrow M
- Alcaraz Maestre J
- Alda Junior WL
- Alexander J
- Aliev T
- Alimena J
- Almeida N
- Alverson G
- Alves GA
- Amapane N
- Amsler C
- Anagnostou G
- Anastassov A
- Anderson J
- Anderson M
- Andrea J
- Andreev V
- Andreev V
- Andreev Y
- Andrews W
- Anghel IM
- Anjos TS
- Antonelli L
- Antunovic Z
- Apanasevich L
- Appelt E
- Apresyan A
- Arce P
- Arcidiacono R
- Arenton MW
- Arfaei H
- Argiro S
- Arneodo M
- Arora S
- Asawatangtrakuldee C
- Asghar MI
- Askew A
- Assran Y
- Ata M
- Attikis A
- Auffray E
- Autermann C
- Auzinger G
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- Azhgirey I
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- Azzolini V
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- Bacchetta N
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- Baden A
- Baeni L
- Baffioni S
- Bagliesi G
- Bai Y
- Baillon P
- Bainbridge R
- Bakhshiansohi H
- Bakirci MN
- Balazs M
- Ball AH
- Ball G
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- Banerjee S
- Banerjee S
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- Banzuzi K
- Barbagli G
- Barberis E
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- Barfuss AF
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- Baumgartel D
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- Piparo D
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- Polatoz A
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- Poll A
- Pollack B
- Pompili A
- Pooth O
- Popov V
- Potenza A
- Potenza R
- Pozdnyakov A
- Pozzobon N
- Prado Da Silva WL
- Primavera F
- Prokofyev O
- Prosper H
- Ptochos F
- Puerta Pelayo J
- Pugliese G
- Puigh D
- Puljak I
- Qazi S
- Qian SJ
- Quan X
- Quast G
- Quertenmont L
- Rabbertz K
- Racz A
- Radburn-Smith BC
- Radi A
- Radicci V
- Radics B
- Ragazzi S
- Rahatlou S
- Rahbaran B
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- Rakness G
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- Rander J
- Ranieri R
- Ranjan K
- Rappoccio S
- Raspereza A
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- Ratnikova N
- Ratti SP
- Raupach F
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- Raymond DM
- Razis PA
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- Redjimi R
- Redondo I
- Reece W
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- Reis T
- Reithler H
- Rekovic V
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- Renker D
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- Reucroft S
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- Riedl C
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- Rizzi A
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- Rodozov M
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- Rolandi G
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- Romeo F
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- Schoerner-Sadenius T
- Schott G
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- Shukla P
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- Silverwood H
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- Sirois Y
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- Sirunyan AM
- Skhirtladze N
- Skuja A
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- Smirnov I
- Smirnov V
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- Troendle D
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- Tyurin N
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- Ujvari B
- Ulmer KA
- Ulrich R
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- Urscheler C
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- Uzunian A
- Vaandering EW
- Valls N
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- Van Remortel N
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- Vanelderen L
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- Vardanyan I
- Varela J
- Varelas N
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- Vartak A
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- Velasco M
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- Velkovska J
- Venturi A
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- Verdini PG
- Veres GI
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- Vergili M
- Verwilligen P
- Verzetti M
- Veszpremi V
- Vesztergombi G
- Veverka J
- Vidal R
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- Villasenor-Cendejas LM
- Villella I
- Vinogradov A
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- Viret S
- Vischia P
- Vishnevskiy D
- Vitulo P
- Vizan Garcia JM
- Vlasov E
- Vlimant JR
- Vodopiyanov I
- Vogel H
- Volkov A
- Volobouev I
- Volodko A
- Volpe R
- Vorobiev I
- Vorobyev A
- Vorobyev A
- Voutilainen M
- Vuosalo C
- Vutova M
- Wagner P
- Wagner SR
- Wagner-Kuhr J
- Wakefield S
- Wallny R
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- Walsh S
- Waltenberger W
- Walzel G
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- Wang M
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- Warchol J
- Wardle N
- Wasserbaech S
- Wayne M
- Weber H
- Weber HA
- Weber M
- Weber M
- Wehrli L
- Weiler T
- Weinberg M
- Wendland L
- Weng Y
- Wenger EA
- Werner JS
- West C
- Wetzel J
- Whitbeck A
- Whitmore J
- Whyntie T
- Wickramage N
- Widl E
- Wilken R
- Wilkinson R
- Williams G
- Williams T
- Willmott C
- Wimpenny S
- Winer BL
- Winn D
- Winstrom L
- Wissing C
- Wittich P
- Wittmer B
- Woehri HK
- Wolf M
- Wolf R
- Womersley WJ
- Won S
- Wood D
- Wood J
- Wood JS
- Worm SD
- Wright D
- Wrochna G
- Wu W
- Wuerthwein F
- Wulz C-E
- Wyslouch B
- Xiao H
- Xie S
- Xu M
- Yagil A
- Yalvac M
- Yang F
- Yang M
- Yang Y
- Yang ZC
- Yazgan E
- Yelton J
- Yetkin T
- Yi K
- Yildirim E
- Yilmaz Y
- Yohay R
- Yoo HD
- Yoo J
- Yoon AS
- York A
- Yu I
- Yu SS
- Yumiceva F
- Yun JC
- Zabel J
- Zabi A
- Zablocki J
- Zaganidis N
- Zakaria M
- Zalewski P
- Zanetti M
- Zang J
- Zarubin A
- Zatserklyaniy A
- Zeinali M
- Zeise M
- Zeuner WD
- Zeyrek M
- Zhang J
- Zhang Z
- Zheng Y
- Zhokin A
- Zhu B
- Zhu RY
- Zhukov V
- Zhukova V
- Ziebarth EB
- Ziegler J
- Zielinski M
- Zito G
- Zotto P
- Zou W
- Zumerle G
- Zuranski A
- Publication venue
- 'American Physical Society (APS)'
- Publication date
- 01/01/2012
- Field of study
The azimuthal anisotropy of charged particles in PbPb collisions at
nucleon-nucleon center-of-mass energy of 2.76 TeV is measured with the CMS
detector at the LHC over an extended transverse momentum (pt) range up to
approximately 60 GeV. The data cover both the low-pt region associated with
hydrodynamic flow phenomena and the high-pt region where the anisotropies may
reflect the path-length dependence of parton energy loss in the created medium.
The anisotropy parameter (v2) of the particles is extracted by correlating
charged tracks with respect to the event-plane reconstructed by using the
energy deposited in forward-angle calorimeters. For the six bins of collision
centrality studied, spanning the range of 0-60% most-central events, the
observed v2 values are found to first increase with pt, reaching a maximum
around pt = 3 GeV, and then to gradually decrease to almost zero, with the
decline persisting up to at least pt = 40 GeV over the full centrality range
measured.Comment: Replaced with published version. Added journal reference and DO
Performance of CMS muon reconstruction in pp collision events at sqrt(s) = 7 TeV
- Author
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- Soares MS
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- Wissing C
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- Woehri HK
- Wolf M
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- Womersley WJ
- Won S
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- Wood J
- Wood JS
- Worm SD
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- Wulz C-E
- Wyslouch B
- Xiao H
- Xie S
- Xu M
- Yagil A
- Yalvac M
- Yang F
- Yang M
- Yang Y
- Yang ZC
- Yazgan E
- Yelton J
- Yetkin T
- Yi K
- Yildirim E
- Yilmaz Y
- Yohay R
- Yoo HD
- Yoo J
- Yoon AS
- York A
- Yu I
- Yu SS
- Yumiceva F
- Yun JC
- Zabel J
- Zabi A
- Zablocki J
- Zaganidis N
- Zakaria M
- Zalewski P
- Zanetti M
- Zang J
- Zang SL
- Zarubin A
- Zatserklyaniy A
- Zeinali M
- Zeise M
- Zeuner WD
- Zeyrek M
- Zhang J
- Zhang Z
- Zheng Y
- Zhokin A
- Zhu B
- Zhu RY
- Zhukov V
- Zhukova V
- Ziebarth EB
- Ziegler J
- Zielinski M
- Zito G
- Zoeller MH
- Zotto P
- Zou W
- Zumerle G
- Zuranski A
- Publication venue
- 'IOP Publishing'
- Publication date
- 01/01/2012
- Field of study
The performance of muon reconstruction, identification, and triggering in CMS
has been studied using 40 inverse picobarns of data collected in pp collisions
at sqrt(s) = 7 TeV at the LHC in 2010. A few benchmark sets of selection
criteria covering a wide range of physics analysis needs have been examined.
For all considered selections, the efficiency to reconstruct and identify a
muon with a transverse momentum pT larger than a few GeV is above 95% over the
whole region of pseudorapidity covered by the CMS muon system, abs(eta) < 2.4,
while the probability to misidentify a hadron as a muon is well below 1%. The
efficiency to trigger on single muons with pT above a few GeV is higher than
90% over the full eta range, and typically substantially better. The overall
momentum scale is measured to a precision of 0.2% with muons from Z decays. The
transverse momentum resolution varies from 1% to 6% depending on pseudorapidity
for muons with pT below 100 GeV and, using cosmic rays, it is shown to be
better than 10% in the central region up to pT = 1 TeV. Observed distributions
of all quantities are well reproduced by the Monte Carlo simulation.Comment: Replaced with published version. Added journal reference and DO
Search for new physics with same-sign isolated dilepton events with jets and missing transverse energy
- Author
- Abbaneo D
- Abbiendi G
- Abbrescia M
- Abdullin S
- Abdulsalam A
- Acosta D
- Acosta JG
- Adair A
- Adam N
- Adam W
- Adams JR
- Adams MR
- Adams T
- Adiguzel A
- Adler V
- Adzic P
- Agram JL
- Aguilar-Benitez M
- Aguilo E
- Ahmad M
- Ahmad WH
- Ahuja S
- Akchurin N
- Akgun B
- Akgun U
- Akin IV
- Alagoz E
- Albajar C
- Albayrak EA
- Albergo S
- Albrow M
- Alcaraz Maestre J
- Alda Junior WL
- Aldaya Martin M
- Alexander J
- Aliev T
- Alimena J
- Almeida N
- Alverson G
- Alves GA
- Amapane N
- Amsler C
- Anagnostou G
- Anastassov A
- Anderson J
- Anderson M
- Andrea J
- Andreev V
- Andreev V
- Andreev Y
- Andrews W
- Anghel IM
- Antonelli L
- Antunovic Z
- Apanasevich L
- Appelt E
- Apresyan A
- Arce P
- Arcidiacono R
- Arenton MW
- Arfaei H
- Argiro S
- Arneodo M
- Arora S
- Asawatangtrakuldee C
- Asghar MI
- Askew A
- Assran Y
- Ata M
- Attikis A
- Auffray E
- Autermann C
- Auzinger G
- Avdeeva E
- Avery P
- Avetisyan A
- Avila C
- Azarkin M
- Azhgirey I
- Aziz T
- Azzi P
- Azzolini V
- Azzurri P
- Baarmand MM
- Babb J
- Bacchetta N
- Bachtis M
- Baden A
- Baeni L
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- Yilmaz Y
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- Zielinski M
- Zito G
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- Zucchetta A
- Zumerle G
- Zuranski A
- Publication venue
- 'American Physical Society (APS)'
- Publication date
- 01/01/2012
- Field of study
A search for new physics is performed in events with two same-sign isolated
leptons, hadronic jets, and missing transverse energy in the final state. The
analysis is based on a data sample corresponding to an integrated luminosity of
4.98 inverse femtobarns produced in pp collisions at a center-of-mass energy of
7 TeV collected by the CMS experiment at the LHC. This constitutes a factor of
140 increase in integrated luminosity over previously published results. The
observed yields agree with the standard model predictions and thus no evidence
for new physics is found. The observations are used to set upper limits on
possible new physics contributions and to constrain supersymmetric models. To
facilitate the interpretation of the data in a broader range of new physics
scenarios, information on the event selection, detector response, and
efficiencies is provided.Comment: Published in Physical Review Letter
Compressed representation of a partially defined integer function over multiple arguments
- Author
- Abbaneo D
- Abbiendi G
- Abbrescia M
- Abdelalim AA
- Abdullin S
- Abdulsalam A
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- Alcaraz Maestre J
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- Publication venue
- Publication date
- 01/01/2013
- Field of study
In OLAP (OnLine Analitical Processing) data are analysed in an n-dimensional cube. The cube may be represented as a partially defined function over n arguments. Considering that often the function is not defined everywhere, we ask: is there a known way of representing the function or the points in which it is defined, in a more compact manner than the trivial one
Performance of CMS muon reconstruction in pp collision events at sqrt(s) = 7 TeV
- Author
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- Yilmaz Y
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- Yun JC
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- Zumerle G
- Zuranski A
- Publication venue
- 'IOP Publishing'
- Publication date
- 01/01/2012
- Field of study
The performance of muon reconstruction, identification, and triggering in CMS
has been studied using 40 inverse picobarns of data collected in pp collisions
at sqrt(s) = 7 TeV at the LHC in 2010. A few benchmark sets of selection
criteria covering a wide range of physics analysis needs have been examined.
For all considered selections, the efficiency to reconstruct and identify a
muon with a transverse momentum pT larger than a few GeV is above 95% over the
whole region of pseudorapidity covered by the CMS muon system, abs(eta) < 2.4,
while the probability to misidentify a hadron as a muon is well below 1%. The
efficiency to trigger on single muons with pT above a few GeV is higher than
90% over the full eta range, and typically substantially better. The overall
momentum scale is measured to a precision of 0.2% with muons from Z decays. The
transverse momentum resolution varies from 1% to 6% depending on pseudorapidity
for muons with pT below 100 GeV and, using cosmic rays, it is shown to be
better than 10% in the central region up to pT = 1 TeV. Observed distributions
of all quantities are well reproduced by the Monte Carlo simulation.Comment: Replaced with published version. Added journal reference and DO
Measurement of jet fragmentation into charged particles in pp and PbPb collisions at sqrt(s[NN]) = 2.76 TeV
- Author
- Abbaneo D
- Abbiendi G
- Abbrescia M
- Abdullin S
- Abdulsalam A
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- Acosta MV
- Adair A
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- Afanasiev S
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- Cumalat JP
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- Cutajar M
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- Czellar S
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- Dabrowski A
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- Temple J
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- Teo WD
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- Thom J
- Thomas L
- Thomas S
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- Ulmer KA
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- Verzetti M
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- Vesztergombi G
- Veverka J
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- Vila I
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- Villasenor-Cendejas LM
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- Vlimant JR
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- Volkov A
- Volobouev I
- Volodko A
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- Vorobiev I
- Vorobyev A
- Vorobyev A
- Voutilainen M
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- Weiler T
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- Yilmaz Y
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- Yoon AS
- York A
- Yu I
- Yu SS
- Yumiceva F
- Yun JC
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- Zabi A
- Zablocki J
- Zaganidis N
- Zakaria M
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- Zeuner WD
- Zeyrek M
- Zhang J
- Zhang Z
- Zheng Y
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- Zhu B
- Zhu RY
- Zhukov V
- Zhukova V
- Zielinski M
- Zito G
- Zotto P
- Zou W
- Zucchetta A
- Zumerle G
- Zuranski A
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2012
- Field of study
Jet fragmentation in pp and PbPb collisions at a centre-of-mass energy of
2.76 TeV per nucleon pair was studied using data collected with the CMS
detector at the LHC. Fragmentation functions are constructed using
charged-particle tracks with transverse momenta pt > 4 GeV for dijet events
with a leading jet of pt > 100 GeV. The fragmentation functions in PbPb events
are compared to those in pp data as a function of collision centrality, as well
as dijet-pt imbalance. Special emphasis is placed on the most central PbPb
events including dijets with unbalanced momentum, indicative of energy loss of
the hard scattered parent partons. The fragmentation patterns for both the
leading and subleading jets in PbPb collisions agree with those seen in pp data
at 2.76 TeV. The results provide evidence that, despite the large parton energy
loss observed in PbPb collisions, the partition of the remaining momentum
within the jet cone into high-pt particles is not strongly modified in
comparison to that observed for jets in vacuum.Comment: Submitted to the Journal of High Energy Physic
Towards a Clinically Relevant Lentiviral Transduction Protocol for Primary Human CD34+ Hematopoietic Stem/Progenitor Cells
- Author
- A Aiuti
- Allison Arndt
- AR Schroder
- C Baum
- C Donaldson
- CE Dunbar
- CI Lee
- DG Miller
- E Montini
- E Prus
- E Vigna
- F Di Nunzio
- F Mazurier
- FD Robart
- FR Santoni de Sio
- G Mostoslavsky
- G Pawelec
- H Glimm
- H Mikkers
- IR Lemischka
- J Barquinero
- J Wilpshaar
- JL Spees
- JS Dando
- K Pike-Overzet
- L Ailles
- L Armstrong
- L Gammaitoni
- L Tuschong
- M Bokhoven
- M Cavazzana-Calvo
- M De Palma
- M Tesio
- Maureen Boyd
- MG Ott
- MH Wu
- Michelle Millington
- MP McCormack
- MS Even
- N Rosenthal
- O Christ
- O Cohen-Haguenauer
- O Tiscornia G Singer
- OS Kustikova
- P Kurre
- R Zufferey
- RE Champlin
- RE Sutto
- RW Storms
- S Barrette
- S Charrier
- SF Williams
- SH Bokman
- SK Nayak
- SO Peter
- Sylvie Shen
- T Dull
- Tanya Applegate
- TY Roe
- U Modlich
- VN Kim
- W Piacibello
- William Giannobile
- WW Ward
- X Li
- X Wu
- Y Cui
- Z Li
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2009
- Field of study
Background: Hematopoietic stem cells (HSC), in particular mobilized peripheral blood stem cells, represent an attractive target for cell and gene therapy. Efficient gene delivery into these target cells without compromising self-renewal and multipotency is crucial for the success of gene therapy. We investigated factors involved in the ex vivo transduction of CD34 + HSCs in order to develop a clinically relevant transduction protocol for gene delivery. Specifically sought was a protocol that allows for efficient transduction with minimal ex vivo manipulation without serum or other reagents of animal origin. Methodology/Principal Findings: Using commercially available G-CSF mobilized peripheral blood (PB) CD34 + cells as the most clinically relevant target, we systematically examined factors including the use of serum, cytokine combinations, prestimulation time, multiplicity of infection (MOI), transduction duration and the use of spinoculation and/or retronectin. A self-inactivating lentiviral vector (SIN-LV) carrying enhanced green fluorescent protein (GFP) was used as the gene delivery vehicle. HSCs were monitored for transduction efficiency, surface marker expression and cellular function. We were able to demonstrate that efficient gene transduction can be achieved with minimal ex vivo manipulation while maintaining the cellular function of transduced HSCs without serum or other reagents of animal origin. Conclusions/Significance: This study helps to better define factors relevant towards developing a standard clinical protocol for the delivery of SIN-LV into CD34 + cells
HIV/HCV Co-infection: Pathogenesis, Clinical Complications, Treatment, and New Therapeutic Technologies
- Author
- A Balagopal
- A d’Arminio Monforte
- A Kovacs
- A Osinusi
- AA Butt
- AA Howard
- AC Tuyama
- AJ Fowell
- Andrea Kovacs
- AY Kim
- B Felipe de
- B Roe
- B Vali
- C Korner
- C Smit
- CH Hinkin
- CL Cherry
- CM Wyatt
- D Nunes
- DB Clifford
- DL Suzman
- DL Thomas
- DP Webster
- E Eynde Van den
- E Tedaldi
- E Vispo
- EC Thomson
- EE Moodie
- EM Martin-Thormeyer
- Eva A. Operskalski
- F Bani-Sadr
- F Collin
- F Poordad
- GD Kirk
- GV Matthews
- H Al-Mohri
- H Izzedine
- H Li
- HA Aronow
- HH Thein
- I Maida
- I Ofotokun
- J Reingold
- J Schulze Zur Wiesch
- JF Pascual-Pareja
- JT Blackard
- K England
- K Neukam
- K Yacisin
- KE Sherman
- KM Marks
- L Al-Harthi
- L Castera
- L Martin-Carbonero
- L Martin-Carbonero
- L Peters
- M Opravil
- M Potter
- M Rodriguez-Torres
- MJ Alter
- MJ Fischer
- MJ Koziel
- MS Sulkowski
- MS Sulkowski
- MV Machado
- N Merchante
- N Nakamoto
- P Ancuta
- P Cicconi
- P Halfon
- P Labarga
- P Labarga
- P Price
- PJ Pockros
- R Bedimo
- RA Tohme
- RK Sterling
- S Letendre
- S Moreno
- S Toma
- S Venkatraman
- S Vergara
- SK Roberts
- ST Shi
- T Frederick
- T Kuntzen
- T Laskus
- T Reiberger
- TW Lapinski
- TY Chen
- V Soriano
- V Soriano
- V Soriano
- VD Gonzalez
- VK Amorosa
- Y Rotman
- Publication venue
- Current Science Inc.
- Publication date
- 01/01/2011
- Field of study
World-wide, hepatitis C virus (HCV) accounts for approximately 130 million chronic infections, with an overall 3% prevalence. Four to 5 million persons are co-infected with HIV. It is well established that HIV has a negative impact on the natural history of HCV, including a higher rate of viral persistence, increased viral load, and more rapid progression to fibrosis, end-stage liver disease, and death. Whether HCV has a negative impact on HIV disease progression continues to be debated. However, following the introduction of effective combination antiretroviral therapy, the survival of coinfected individuals has significantly improved and HCV-associated diseases have emerged as the most important co-morbidities. In this review, we summarize the newest studies regarding the pathogenesis of HIV/HCV coinfection, including effects of coinfection on HIV disease progression, HCV-associated liver disease, the immune system, kidney and cardiovascular disease, and neurologic status; and effectiveness of current anti-HIV and HCV therapies and proposed new treatment strategies
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