Infection

CAR T cell therapies may lead to reactivation of childhood viral infections

Posted on by yun
14
Nov
<div data-thumb="https://scx1.b-cdn.net/csz/news/tmb/2023/car-t-cell-therapies-m.jpg" data-src="https://scx2.b-cdn.net/gfx/news/hires/2023/car-t-cell-therapies-m.jpg" data-sub-html="Petabase-scale analysis of viral nucleic acids reveals that HHV-6 is reactivated in human T cells. a, Schematic of life cycles of endogenous human viruses. Viruses can enter a latent phase after primary infection and become reactivated following environmental cues, including drugs, immunization and other infections. b, Enumeration of BioSamples with human viruses showing signs of reactivation based on expressed viral nucleic acids in human Sequence Read Archive samples. c, Proportion of BioSamples with viral transcriptional expression annotated as T cells. These eight viruses showed evidence of reactivation specifically in T cells whereas the remaining viruses from b showed no such evidence of reactivation. d, Reanalysis of RNA-seq data from ref. 22. CD4+ T cells from three separate donors were either infected with HIV or mock infected and cultured for about 2 weeks. Shown is the percentage of RNA molecules aligning to the HHV-6B reference transcriptome e, Reanalysis of the data from ref. 18. Naive and memory CD4+ T cells were separated and cultured for 2 weeks. Shown is the percentage of RNA molecules aligning to the HHV-6B reference transcriptome. f, Quantification of HHV-6B episomal DNA from a reanalysis of ChIP–seq data from ref. 18. Shown are the percentages of DNA reads uniquely mapping to the HHV-6B transcriptome, noting the percentage of total DNA reads mapping to the HHV-6B reference genome. g, Coverage of the HHV-6B genome across two ChIP–seq libraries from different donors from ref. 18. Repetitive regions on the ends of the chromosome show no uniquely mapping reads. Credit: Nature (2023). DOI: 10.1038/s41586-023-06704-2″>

Petabase-scale analysis of viral nucleic acids reveals that HHV-6 is reactivated in human T cells. a, Schematic of life cycles of endogenous human viruses. Viruses can enter a latent phase after primary infection and become reactivated following environmental cues, including drugs, immunization and other infections. b, Enumeration of BioSamples with human viruses showing signs of reactivation based on expressed viral nucleic acids in human Sequence Read Archive samples. c, Proportion of BioSamples with viral transcriptional expression annotated as T cells. These eight viruses showed evidence of reactivation specifically in T cells whereas the remaining viruses from b showed no such evidence of reactivation. d, Reanalysis of RNA-seq data from ref. 22. CD4+ T cells from three separate donors were either infected with HIV or mock infected and cultured for about 2 weeks. Shown is the percentage of RNA molecules aligning to the HHV-6B reference transcriptome e, Reanalysis of the data from ref. 18. Naive and memory CD4+ T cells were separated and cultured for 2 weeks. Shown is the percentage of RNA molecules aligning to the HHV-6B reference transcriptome. f, Quantification of HHV-6B episomal DNA from a reanalysis of ChIP–seq data from ref. 18. Shown are the percentages of DNA reads uniquely mapping to the HHV-6B transcriptome, noting the percentage of total DNA reads mapping to the HHV-6B reference genome. g, Coverage of the HHV-6B genome across two ChIP–seq libraries from different donors from ref. 18. Repetitive regions on the ends of the chromosome show no uniquely mapping reads. Credit: Nature (2023). DOI: 10.1038/s41586-023-06704-2

Research led by the Department of Pathology at Stanford University, California, has found that chimeric antigen receptor T (CAR T) cell therapy can potentially result in a reactivation of human herpesvirus 6 (HHV-6) by CAR T cells in patients.

In a paper titled “Latent human herpesvirus 6 is reactivated in CAR T cells,” published in Nature, the team gathered previous data surrounding CAR T therapy studies to investigate the in vivo reactivation of HHV-6 by CAR T cells in patients receiving CAR T cell therapy. The study sought to characterize the phenomenon of HHV-6 reactivation, particularly in the context of CAR T cell treatment for B cell lymphoma or leukemia.

A reanalysis of scRNA-seq datasets from three cohorts of patients receiving autologous CAR T cell products was conducted. While no HHV-6 viral transcripts were detected in pre-infusion products, a significant increase in HHV-6+ cells was observed in post-infusion samples.

The study identified 28 cells expressing HHV-6B transcripts in post-infusion samples, with 13 resembling rare “super-expressor” cells among research-grade allogeneic CAR T cells. Detailed time course analysis of two patients with super-expressors revealed the presence of HHV-6+ cells a week into treatment, coinciding with clinical symptoms of immune effector-associated neurotoxicity syndrome. The symptoms, such as delirium and neurocognitive decline, align with HHV-6 viral presence in blood, though it may not be causal for all patients.

These findings suggest a link between T cell activation, proliferation, and culture duration with HHV-6 reactivation, emphasizing the need for further consideration in developing and monitoring CAR T cell therapies.

The study also found incidents of HHV-6B reactivation in standard CD4+ T cell cultures, confirming the potential association between cell therapy products and lytic HHV-6 infection that had been reported in clinical trials of CAR T.

Human herpesvirus 6B is nearly universally acquired (approximately 70%) by age three and causes a common childhood illness called exanthema subitum or roseola infantum. By adulthood, approximately 95% of people have encountered the virus. The virus is present in multiple cell and tissue types during primary infection, and the viral DNA continues to survive post-infection in peripheral blood mononuclear cells.

The authors emphasize the utility of comprehensive genomics analyses in implicating cell therapy products as potential sources contributing to viral infections. The correlation between HHV-6 reactivation and CAR T treatments raises the possibility of other latent viral reactivations across various cell therapies and suggests more investigation is required.

More information:
Caleb A. Lareau et al, Latent human herpesvirus 6 is reactivated in CAR T cells, Nature (2023). DOI: 10.1038/s41586-023-06704-2

© 2023 Science X Network

Citation:
CAR T cell therapies may lead to reactivation of childhood viral infections (2023, November 14)
retrieved 14 November 2023
from https://medicalxpress.com/news/2023-11-car-cell-therapies-reactivation-childhood.html

This document is subject to copyright. Apart from any fair dealing for the purpose of private study or research, no
part may be reproduced without the written permission. The content is provided for information purposes only.

yun

Leave a Reply

Your email address will not be published. Required fields are marked *