Prospective virological follow‐up of hepatitis C infection in a haemodialysis unit

1998 ◽  
Vol 5 (2) ◽  
pp. 115-121 ◽  
Author(s):  
P. Halfon ◽  
H. Khiri ◽  
J. M. Feryn ◽  
C. Sayada ◽  
M. Chanas ◽  
...  
Author(s):  
Tanvi Khera ◽  
Yanqin Du ◽  
Daniel Todt ◽  
Katja Deterding ◽  
Benedikt Strunz ◽  
...  

Abstract Background Treatment with direct acting antivirals (DAAs) in patients with chronic hepatitis C infection leads to partial restoration of soluble inflammatory mediators (SIMs). In contrast, we hypothesized that early DAA treatment of acute hepatitis C with DAAs may normalize most SIMs. Methods In this study, we made use of a unique cohort of acute symptomatic hepatitis C who cleared HCV with a 6-week course of ledipasvir/sofosbuvir. Plasma samples were used for proximity extension assay (PEA) measuring 92 proteins. Results Profound SIM alterations were observed in acute HCV patients, with marked upregulation of IL-6 and CXCL10 while certain mediators were down-regulated (e.g. MCP-4, IL-7). During treatment and follow-up, the majority of SIMs decreased but not all normalized (e.g. CDCP1, IL-18). Of note, SIMs that were down-regulated before DAA treatment remained suppressed while others that were initially unchanged, declined to lower values during treatment and follow-up (e.g.CD244). Conclusions Acute hepatitis C was associated with marked changes in the soluble inflammatory milieu as compared to both chronic hepatitis patients and healthy controls. Whereas early DAA treatment partly normalized this altered signature, long-lasting imprints of HCV remained. Thus, acute HCV-induced changes in the immune system may persist even after a short duration of viremia.


Renal Failure ◽  
2004 ◽  
Vol 26 (5) ◽  
pp. 583-588 ◽  
Author(s):  
Fatma Nurhan Ozdemir ◽  
Ali Akcay ◽  
Siren Sezer ◽  
Sedat Boyacioglu ◽  
Binnaz Handan Ozdemir ◽  
...  

PLoS ONE ◽  
2017 ◽  
Vol 12 (10) ◽  
pp. e0185609 ◽  
Author(s):  
Swee Lin G. Chen Yi Mei ◽  
Alexander J. Thompson ◽  
Britt Christensen ◽  
Georgina Cunningham ◽  
Lucy McDonald ◽  
...  

2012 ◽  
Vol 93 (4) ◽  
pp. 450-453 ◽  
Author(s):  
Isabel Campos-Varela ◽  
Lluis Castells ◽  
Juan Ignacio Esteban ◽  
Marta Bes ◽  
Francisco Rodríguez-Frías ◽  
...  

Addiction ◽  
2005 ◽  
Vol 100 (6) ◽  
pp. 820-828 ◽  
Author(s):  
Kate A. Dolan ◽  
James Shearer ◽  
Bethany White ◽  
Jialun Zhou ◽  
John Kaldor ◽  
...  

Hepatology ◽  
1999 ◽  
Vol 29 (3) ◽  
pp. 908-914 ◽  
Author(s):  
Stephen A. Villano ◽  
David Vlahov ◽  
Kenrad E. Nelson ◽  
Sylvia Cohn ◽  
David L. Thomas

2021 ◽  
Author(s):  
Anthony E Ades ◽  
Fabiana Gordon ◽  
Karen Scott ◽  
Jeannie Collins ◽  
Claire Thorne ◽  
...  

Background. Current guidelines recommend that infants born to women with hepatitis C (HCV) viremia are screened for HCV antibody at age 18 months, and if positive, referred for RNA testing at 3 years to confirm chronic infection. This policy is based in part on analyses suggesting 25%-40% of vertically acquired HCV infections clear spontaneously within 4-5 years. Methods. Data on 179 infants with RNA and/or anti-HCV evidence of vertically acquired viraemia (single PCR+) or confirmed infection (2 PCR+ or anti-HCV beyond 18 months) in three prospective European cohorts were investigated. Ages at clearance of viremia and confirmed infection were estimated taking account of interval censoring and delayed entry. We also investigated clearance in infants in whom RNA was not detectable until after 6 weeks. Results. Clearance rates decline rapidly over the first 6 months. An estimated 90.6% (95%CrI: 83.5-95.9) of viremia cleared by 5 years, most within 3 months, and 65.9% (50.1-81.6) of confirmed infection cleared by 5 years, at a median 12.4 (7.1-18.9) months. If treatment began at age 6 months, 18 months or 3 years, at least 59.0% (42.0-76.9), 39.7 (17.9-65.9), and 20.9 (4.6-44.8) of those treated would clear without treatment. In seven (6.6%) confirmed infections, RNA was not detectable until after 6 weeks, and in 2 (1.9%) not until after 6 months. However, all such cases subsequently cleared. Conclusions. Most viraemia clears within 3 months, and most confirmed infection by 3 years. Delaying treatment avoids but does not eliminate over-treatment and should be balanced against loss to follow-up.


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