4.7 Article

Cytomegalovirus-specific neutralizing antibodies effectively prevent uncontrolled infection after allogeneic hematopoietic stem cell transplantation

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ISCIENCE
卷 25, 期 10, 页码 -

出版社

CELL PRESS
DOI: 10.1016/j.isci.2022.105065

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资金

  1. Genergy Biotechnology of Shanghai
  2. National Natural Science Foundation of China [81903637, 82100230]
  3. Key Projects of Research and Development Program of Anhui Province [201904a07020094]
  4. Fundamental Research Funds for the Central Universities in China [WK9110000001, WK9110000027, WK9110000168]

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This study compared the immune cells of patients with controlled and uncontrolled CMV infection after allo-HSCT. It found that patients with uncontrolled infection had insufficient B-cells due to impaired B-cell reconstitution. In contrast, patients with controlled infection had reconstructed B-cells showing mature B-cell characteristics and enrichment of CMV-associated B-cell receptors. Additionally, the controlled infection group had higher levels of anti-CMV-specific immunoglobulin G (IgG) in their serum, which could effectively inhibit CMV infection. These findings highlight the importance of B-cells and anti-CMV-specific neutralizing IgGs in controlling CMV infection post-allo-HSCT and suggest their potential as a supplementary treatment for improved outcomes.
Cytomegalovirus (CMV) infection remains one of the most frequent and life-threatening infectious complications after allogeneic hematopoietic stem cell transplantation (allo-HSCT). Herein, we comprehensively compared the immune cells of patients with uncontrolled and controlled :MV infection post-allo-HSCT and found that B-cells were extraordinarily insufficient because of impaired B-cells reconstitution in the uncontrolled infection group. Furthermore, in the controlled infection group, reconstructed B-cells showed signatures of mature B-cells, high expression of CXCR4 and IFITM1, and enrichment of CMV-associated B-cell receptors, which were lacking in the uncontrolled infection group. Consistently, sera from the uncontrolled infection group failed to inhibit CMV infection via neutralizing virus in vitro because of its lower content of anti-CMV-specific immunoglobulin G (IgG) than the controlled infection group. Overall, these results highlighted the contribution of B cells and anti-CMV-specific neutralizing IgGs to the restraint of CMV infection post-allo-HSCT, suggesting their potential as a supplementary treatment to improve outcomes.

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