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February 8, 2026Immunology0 citationsOpen Access

Latent Neoehrlichia mikurensis Infections May Be Reactivated in Patients With B‐Cell Lymphomas Treated With Rituximab

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LWLinda WassCLCatharina LewerinDJDaniel Jaén‐Luchoro

Key Points

  • The aim was to explore whether latent Neoehrlichia mikurensis infections reactivate in patients with B-cell lymphomas treated with rituximab.
  • Evaluated 97 patients with B-cell lymphomas treated with rituximab
  • Determined incidence of N. mikurensis reactivation
  • Assessed presence of N. mikurensis-specific T cells in latently infected individuals
  • 4% of patients reactivated N. mikurensis infection
  • 4% had asymptomatic infection prior to treatment
  • Infected patients showed N. mikurensis-specific T cells and up-regulated markers like CXCL10 and IFN-γ
  • Expanded γδ T-cell populations were present in infected lymphoma patients

Abstract

ABSTRACT The intracellular, tick‐borne bacterium Neoehrlichia (N.) mikurensis can cause neoehrlichiosis in patients with compromised B‐cell defences, while immunocompetent individuals are frequently healthy carriers of the infection. We hypothesised that N. mikurensis induces latent infections that reactivate when B‐cell immunity is compromised. We tested this hypothesis by determining the incidence of N. mikurensis reactivation in 97 patients with B‐cell lymphomas who were treated with anti‐CD20 antibody therapy (rituximab) and evaluating the presence of N. mikurensis ‐specific T cells in latently infected individuals. Four patients (4%) reactivated N. mikurensis infection and four patients (4%) had asymptomatic infection before the initiation of B‐cell suppression. All eight patients who were infected with N. mikurensis had N. mikurensis ‐specific, perforin‐expressing Th1 and CD8+ T‐cell populations with up‐regulation of CXCL10 and IFN‐γ, in contrast to the noninfected lymphoma patients who lacked these T‐cell subsets. The infected lymphoma patients also had expanded γδ T‐cell populations. This study supports the notion of latent, reactivatable N. mikurensis infections.

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Cite This Study

Wass et al. (2026) studied this question.

synapsesocial.com/papers/6988292d0fc35cd7a88494b4https://doi.org/10.1111/imm.70120
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