Abstract

Human T lymphotropic virus type 1 (HTLV-1) is endemic in the southern part of Japan. Infection of the virus can cause adult T cell leukemia/lymphoma (ATL), while most infected individuals remain in a carrier state for a long period of time. Although rare cases of carriers, like ATL patients, who developed opportunistic infections, have been reported, hematological changes of carriers who are prone to opportunistic infections have not been well defined. Here, we present a case of an HTLV-1 carrier who developed Mycobacterium intracellulare infection and Pneumocystis jirovecii pneumonia (PcP) simultaneously. Flow cytometric analysis of bone marrow cells revealed an aberrant compositional change similar to that in ATL patients. This suggests the presence of a pre-ATL state prior to the development of ATL, which is notable in terms of underlying cellular immunodeficiency.

Highlights

  • HITV-1 is an endemic retrovirus and infects CD4+ T cells

  • We present a case of an Human T lymphotropic virus type 1 (HTLV-1) carrier who developed Mycobacterium intracellulare infection and Pneumocystis jirovecii pneumonia (PcP) simultaneously

  • The proportion of CD4+CD25+ T cells was aberrantly increased in her bone marrow samples, which is characteristically seen in adult T cell leukemia/lymphoma (ATL) patients

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Summary

Introduction

A part of HTLV-1infected patients develop ATL, who often suffer from opportunistic infections due to cellular immunodeficiency. Carriers have been reported to develop opportunistic infections. Immune state of carriers has not been clarified compared with that of ATL patients. We present a case of an HTLV-1 carrier who developed Mycobacterium intracellulare infection and Pneumocystis jirovecii pneumonia simultaneously. The proportion of CD4+CD25+ T cells was aberrantly increased in her bone marrow samples, which is characteristically seen in ATL patients. This implies the presence of a pre-ATL state in carriers based on their immunological changes, which is clinically relevant because of their immunodeficiency

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