Late effects of total body irradiation on hematopoietic recovery and immune function in rhesus macaques.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2019
Historique:
received: 18 06 2018
accepted: 28 12 2018
entrez: 14 2 2019
pubmed: 14 2 2019
medline: 31 10 2019
Statut: epublish

Résumé

While exposure to radiation can be lifesaving in certain settings, it can also potentially result in long-lasting adverse effects, particularly to hematopoietic and immune cells. This study investigated hematopoietic recovery and immune function in rhesus macaques Cross-sectionally (at a single time point) 2 to 5 years after exposure to a single large dose (6.5 to 8.4 Gray) of total body radiation (TBI) derived from linear accelerator-derived photons (2 MeV, 80 cGy/minute) or Cobalt 60-derived gamma irradiation (60 cGy/min). Hematopoietic recovery was assessed through measurement of complete blood counts, lymphocyte subpopulation analysis, and thymus function assessment. Capacity to mount specific antibody responses against rabies, Streptococcus pneumoniae, and tetanus antigens was determined 2 years after TBI. Irradiated macaques showed increased white blood cells, decreased platelets, and decreased frequencies of peripheral blood T cells. Effects of prior radiation on production and export of new T cells by the thymus was dependent on age at the time of analysis, with evidence of interaction with radiation dose for CD8+ T cells. Irradiated and control animals mounted similar mean antibody responses to proteins from tetanus and rabies and to 10 of 11 serotype-specific pneumococcal polysaccharides. However, irradiated animals uniformly failed to make antibodies against polysaccharides from serotype 5 pneumococci, in contrast to the robust responses of non-irradiated controls. Trends toward decreased serum levels of anti-tetanus IgM and slower peak antibody responses to rabies were also observed. Taken together, these data show that dose-related changes in peripheral blood cells and immune responses to both novel and recall antigens can be detected 2 to 5 years after exposure to whole body radiation. Longer term follow-up data on this cohort and independent validation will be helpful to determine whether these changes persist or whether additional changes become evident with increasing time since radiation, particularly as animals begin to develop aging-related changes in immune function.

Identifiants

pubmed: 30759098
doi: 10.1371/journal.pone.0210663
pii: PONE-D-18-18177
pmc: PMC6373904
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0210663

Subventions

Organisme : NIA NIH HHS
ID : P30 AG049638
Pays : United States
Organisme : NIH HHS
ID : S10 OD018164
Pays : United States
Organisme : NIAID NIH HHS
ID : U19 AI067798
Pays : United States
Organisme : NIAID NIH HHS
ID : UC6 AI058607
Pays : United States

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Laura P Hale (LP)

Department of Pathology and Duke Human Vaccine Institute, Duke University School of Medicine, Durham, NC, United States of America.

Gowrisankar Rajam (G)

Immunobiology Laboratory, Centers for Disease Control and Prevention (CDC), Atlanta, GA, United States of America.

George M Carlone (GM)

Immunobiology Laboratory, Centers for Disease Control and Prevention (CDC), Atlanta, GA, United States of America.

Chen Jiang (C)

Duke Cancer Institute, Duke University Medical Center, Durham, NC, United States of America.

Kouros Owzar (K)

Duke Cancer Institute, Duke University Medical Center, Durham, NC, United States of America.
Department of Biostatistics and Bioinformatics, Duke University Medical Center, Durham, NC, United States of America.

Greg Dugan (G)

Department of Pathology, Section on Comparative Medicine, Wake Forest School of Medicine, Winston-Salem, NC, United States of America.

David Caudell (D)

Department of Pathology, Section on Comparative Medicine, Wake Forest School of Medicine, Winston-Salem, NC, United States of America.

Nelson Chao (N)

Department of Medicine, Duke University School of Medicine, Durham, NC, United States of America.

J Mark Cline (JM)

Department of Pathology, Section on Comparative Medicine, Wake Forest School of Medicine, Winston-Salem, NC, United States of America.

Thomas C Register (TC)

Department of Pathology, Section on Comparative Medicine, Wake Forest School of Medicine, Winston-Salem, NC, United States of America.

Gregory D Sempowski (GD)

Department of Pathology and Duke Human Vaccine Institute, Duke University School of Medicine, Durham, NC, United States of America.
Department of Medicine, Duke University School of Medicine, Durham, NC, United States of America.

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