This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow E-mail this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Kaur, I.
Right arrow Articles by Pierson, D. L.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kaur, I.
Right arrow Articles by Pierson, D. L.

 Previous Article  |  Next Article 

Clinical and Vaccine Immunology, October 2008, p. 1523-1528, Vol. 15, No. 10
1071-412X/08/$08.00+0     doi:10.1128/CVI.00065-08
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Effect of Spaceflight on Ability of Monocytes To Respond to Endotoxins of Gram-Negative Bacteria{triangledown}

Indreshpal Kaur,1* Elizabeth R. Simons,2 Asha S. Kapadia,3 C. Mark Ott,4 and Duane L. Pierson4

Enterprise Advisory Services Inc., Houston, Texas,1 Department of Biochemistry, Boston University School of Medicine, Boston, Massachusetts,2 School of Public Health, University of Texas Health Science Center, Houston, Texas,3 NASA Johnson Space Center, Houston, Texas4

Received 5 February 2008/ Returned for modification 28 March 2008/ Accepted 21 August 2008

Astronauts live and work in relatively crowded, confined environments on the Space Shuttle and the International Space Station. They experience a unique set of stressors that contribute to a diminishment of many immune responses. This study investigated the ability of the shuttle crew members' monocytes to respond to gram-negative endotoxin that they could encounter during infections. Blood specimens were collected from 20 crew members and 15 control subjects 10 days before launch, 3 to 4 h after landing, and 15 days after landing and from crew members during their annual medical examination at 6 to 12 months after landing. When challenged with gram-negative endotoxin, the crew member's monocytes collected at all three time points produced lower levels of interleukin-6 (IL-6) and IL-1β and higher levels of IL-1ra and IL-8 compared to those of control subjects. Cytokines were assessed by measuring the number of cells positive for intracellular cytokines. These values returned to normal 6 to 12 months after landing, except for IL-1ra, which was still higher (five- to sixfold) than in controls. This phenomenon was accompanied by an increased expression of Toll-like receptor 4 and decreased expression of CD14 on the crew members' monocytes at all time points. There were also increased levels of the lipopolysaccharide binding protein in the plasma of the crew members 3 to 4 h and 15 days after landing. This study shows that spaceflight-associated factors (in-flight and preflight) modulate the response of monocytes to gram-negative endotoxins.

* Corresponding author. Present address: Department of Stem Cell Transplantation and Cellular Therapy, Box 65, University of Texas M. D. Anderson Cancer Center, 1515 Holcombe Blvd., Houston, TX 77030. Phone: (713) 563-4811. Fax: (713) 563-4825. E-mail: ikaur{at}mdanderson.org

{triangledown} Published ahead of print on 3 September 2008.

Clinical and Vaccine Immunology, October 2008, p. 1523-1528, Vol. 15, No. 10
1071-412X/08/$08.00+0     doi:10.1128/CVI.00065-08
Copyright © 2008, American Society for Microbiology. All Rights Reserved.



This article has been cited by other articles:

  • Gueguinou, N., Huin-Schohn, C., Bascove, M., Bueb, J.-L., Tschirhart, E., Legrand-Frossi, C., Frippiat, J.-P. (2009). Could spaceflight-associated immune system weakening preclude the expansion of human presence beyond Earth's orbit?. J. Leukoc. Biol. 86: 1027-1038 [Abstract] [Full Text]  


Copyright © 2010 by the American Society for Microbiology.   For an alternate route to Journals.ASM.org, visit: http://intl-journals.asm.org | More Info»