02465nas a2200301 4500000000100000008004100001260001200042653003400054653003500088653002100123653001000144653001800154653002700172100001100199700001300210700001200223700001500235700001100250700001200261700001200273700001100285245018600296856007700482300000900559490000700568520157400575022001402149 2026 d c02/202610aClinico-epidemiological study10adapsone-induced hypersentivity10aLeprosy patients10aNepal10aHerpesviridae10aMolecular Epidemiology1 aRana D1 aShakya J1 aBaral S1 aShrestha R1 aKoju K1 aJoshi J1 aHagge D1 aShah M00aClinico-Epidemiological and Molecular Evidences for Reactivation of Herpesviruses in Dapsone-Induced Hypersensitivity Reactions in Nepalese Leprosy Patients: An Observational Study. uhttps://pmc.ncbi.nlm.nih.gov/articles/PMC12933410/pdf/IID3-14-e70385.pdf a1-130 v143 a
INTRODUCTION:
Dapsone hypersensitivity (DHS) is a potentially fatal and severe cutaneous adverse reaction that occurs in patients taking dapsone. As leprosy, for which dapsone is used as part of multidrug therapy, usually occurs in countries with resource limitations, the morbidity and mortality caused by DHS are more dreadful. Herpesviruses (especially HHV-5 and 6) are frequently associated with the etiology of drug-induced hypersensitivity reactions, and the reactivation of these viruses coincides with the reflare of clinical symptoms even after the cessation of culprit drugs.
METHODS:
We reviewed the hospital charts of patients (Cohort 1) with DHS who were admitted to our hospital at the time of the DHS episode. Similarly, we examined the presence of HHV-5 and 6 in another independent group of DHS blood samples (Cohort 2) by PCR.
RESULTS:
Seventy-one percent (71%, 17/24) of DHS patients experienced recrudescence (reflare) of symptoms ~20 days after cessation of dapsone in Cohort 1. In Cohort 2, 39% (13/33) of blood samples from DHS patients showed the presence of at least one herpesvirus.
CONCLUSION:
In this exploratory study, our data suggest the role of herpesviruses in the natural history of DHS and identify patterns that support future hypothesis-driven investigations into antiviral treatment strategies for the management of DHS cases, with the potential to reduce morbidity and mortality.
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