Herpesvirus Screening in Childhood Hematopoietic Transplant Reveals High Systemic Inflammation in Episodes of Multiple Viral Detection and an EBV Association with Elevated IL-1 beta, IL-8 and Graft-Versus-Host Disease


Por: Rojas-Rechy, Moises H., Gaytan-Morales, Felix, Sanchez-Ponce, Yessica, Castorena-Villa, Ivan, Lopez-Martinez, Briceida, Parra-Ortega, Israel, Escamilla-Nunez, Maria C., Mendez-Tenorio, Alfonso, Pompa-Mera, Ericka N., Martinez-Ruiz, Gustavo U., Fuentes-Panana, Ezequiel M., Morales-Sanchez, Abigail

Publicada: 1 ago 2022
Resumen:
Infections remain a major cause of morbidity and mortality among hematopoietic stem cell transplant (HSCT) recipients. Unlike Epstein-Barr Virus (EBV) and Human Cytomegalovirus (HCMV), Human Herpesvirus (HHV) 6, HHV7 and HHV8 are not routinely monitored in many centers, especially in the pediatric population of low-medium income countries. We screened EBV, HCMV, HHV6, HHV7 and HHV8 in 412 leukocytes-plasma paired samples from 40 pediatric patients assisted in a tertiary hospital in Mexico. Thirty-two underwent allo-HSCT, whereas eight received auto-HSCT. Overall viral detection frequencies in allo- and auto-HSCT were: EBV = 43.7% and 30.0%, HCMV = 5.0% and 6.7%, HHV6 = 7.9% and 20.0% and HHV7 = 9.7% and 23.3%. HHV8 was not detected in any sample. Interestingly, HHV6 and HHV7 were more frequent in auto-HSCT, and HHV6 was observed in all episodes of multiple detection in auto-HSCT patients. We found EBV DNA in plasma samples, whereas HCMV, HHV6 and HHV7 DNA were predominantly observed in leukocytes, indicative of their expansion in cellular compartments. We also found that IL-1 beta, IL-2, IL-6 and IL-8 were significantly increased in episodes in which multiple viruses were simultaneously detected, and samples positive for EBV DNA and graft-versus-host disease had a further increase of IL-1 beta and IL-8. In conclusion, the EBV, HCMV, HHV6 and HHV7 burdens were frequently detected in allo- and auto-HSCT, and their presence associated with systemic inflammation.

Filiaciones:
Rojas-Rechy, Moises H.:
 Childrens Hosp Mexico Federico Gomez, Res Unit Virol & Canc, Mexico City 06720, DF, Mexico

 Natl Polytech Inst, Postgrad Program Biomed & Mol Biotechnol, Mexico City 11340, DF, Mexico

Gaytan-Morales, Felix:
 Childrens Hosp Mexico Federico Gomez, Bone Marrow Transplant Serv, Mexico City 06720, DF, Mexico

Sanchez-Ponce, Yessica:
 Childrens Hosp Mexico Federico Gomez, Res Unit Virol & Canc, Mexico City 06720, DF, Mexico

Castorena-Villa, Ivan:
 Childrens Hosp Mexico Federico Gomez, Bone Marrow Transplant Serv, Mexico City 06720, DF, Mexico

Lopez-Martinez, Briceida:
 Childrens Hosp Mexico Federico Gomez, Subdirect Diagnost Auxiliary Serv, Mexico City 06720, DF, Mexico

Parra-Ortega, Israel:
 Childrens Hosp Mexico Federico Gomez, Dept Clin Lab, Mexico City 06720, DF, Mexico

Escamilla-Nunez, Maria C.:
 Natl Inst Publ Hlth, Cuernavaca 62100, Morelos, Mexico

Mendez-Tenorio, Alfonso:
 Inst Politecn Nacl, Lab Biotecnol & Bioinformat Genom, Escuela Nacl Ciencias Biol, Mexico City 11340, DF, Mexico

Pompa-Mera, Ericka N.:
 Mexican Inst Social Secur IMSS, Natl Med Ctr CMN SIGLO XXI, Pediat Hosp, Infect & Parasit Dis Med Res Unit UIMEIP, Mexico City 06720, DF, Mexico

Martinez-Ruiz, Gustavo U.:
 Univ Nacl Autonoma Mexico, Fac Med, Div Invest, Mexico City 04510, DF, Mexico

 Childrens Hosp Mexico Federico Gomez, Lab Invest Patol Expt, Mexico City 06720, DF, Mexico

Fuentes-Panana, Ezequiel M.:
 Childrens Hosp Mexico Federico Gomez, Res Unit Virol & Canc, Mexico City 06720, DF, Mexico

Morales-Sanchez, Abigail:
 Childrens Hosp Mexico Federico Gomez, Res Unit Virol & Canc, Mexico City 06720, DF, Mexico
ISSN: 20762607
Editorial
MDPI, ST ALBAN-ANLAGE 66, CH-4052 BASEL, SWITZERLAND, Suiza
Tipo de documento: Article
Volumen: 10 Número: 8
Páginas:
WOS Id: 000846521900001
ID de PubMed: 36014102
imagen Green Accepted, gold, All Open Access, Gold, Green

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