Skip Navigation


Hum. Reprod. Advance Access originally published online on June 3, 2004
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF ) Freely available
Right arrow All Versions of this Article:
19/7/1554    most recent
deh275v1
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (2)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Maertens, A.
Right arrow Articles by Levy, R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Maertens, A.
Right arrow Articles by Levy, R.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Human Reproduction, Vol. 19, No. 7, 1554-1557, July 2004
© 2004 European Society of Human Reproduction and Embryology

Validation of safety procedures for the cryopreservation of semen contaminated with hepatitis C virus in assisted reproductive technology

A. Maertens1, T. Bourlet1, N. Plotton1, B. Pozzetto1 and R. Levy2,3

1 Laboratoire de Bactériologie-Virologie and 2 Laboratoire de Biologie de la Reproduction, GIMAP, University Hospital of Saint-Etienne, 42055 Saint-Etienne, France

3 To whom correspondence should be addressed. e-mail: rachel.levy{at}chu-st-etienne.fr

BACKGROUND: In France, assisted reproductive technologies involving a hepatitis C virus (HCV)-infected man requires the cryopreservation of potentially infected semen (in order to establish the presence of HCV), hence the need for a safe and secure storage system. We evaluated the safety of high-security straws for the conservation of semen containing HCV RNA under routine conditions. METHODS: Ionomeric resin (IR) straws were filled with seminal plasma spiked with different concentrations of HCV RNA and sealed using a thermo-solder. After a 4% sodium hypochlorite treatment and/or cryopreservation for 7 days in liquid nitrogen, the outside ends of each straw were rinsed with RNAse-free water. RESULTS: No HCV RNA could be detected in any of the water samples. Additional samples included the rinsing water from straws sealed by thermo-solder and from the heating wire used to cut the end of straws containing HCV-positive semen. The latter samples were found positive for both HCV RNA and the protamine-2 gene expressed by spermatozoa. CONCLUSIONS: These results demonstrate the safety of IR straws, the filling system and the thermo-solder for cryopreservation of semen containing HCV in liquid nitrogen. Decontamination of the straw after sealing and the use of disposable scissors to open the straws are strongly recommended.

Key words: assisted reproductive technology/cryopreservation/hepatitis C virus/straws/viral safety


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Hum ReprodHome page
A. Bielanski and G. Vajta
Risk of contamination of germplasm during cryopreservation and cryobanking in IVF units
Hum. Reprod., October 1, 2009; 24(10): 2457 - 2467.
[Abstract] [Full Text] [PDF]


Home page
ESHRE MonogrHome page
C. Huyser
Affordable ART services in Africa: synthesis and adaptation of laboratory services
ESHRE Monogr, July 1, 2008; 2008(1): 77 - 84.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.