Use of interferon gamma following prrimary graft failure after hematopoietic stem cell transplantation in a patient with chronic granulomatous disease in a public hospital in Peru: a case report

Authors

  • Pedro Ruiz Hospital Nacional Edgardo Rebagliati Martins, Servicio de Inmunología y Alergia. Lima, Perú. Médico residente de inmunología y alergia. https://orcid.org/0000-0002-8520-3223
  • Paola Stephanie Alegre Yataco Hospital Nacional Edgardo Rebagliati Martins, Servicio de Inmunología y Alergia. Lima, Perú. Médico residente de inmunología y alergia. https://orcid.org/0009-0007-1455-8004
  • Fernando Rubén Rivera Castillo Hospital Nacional Edgardo Rebagliati Martins, Servicio de Inmunología y Alergia. Lima, Perú. Médico residente de inmunología y alergia. https://orcid.org/0009-0006-3014-0057
  • Juan Carlos Aldave Becerra Hospital Nacional Edgardo Rebagliati Martins, Servicio de Inmunología y Alergia. Lima, Perú. Médico residente de inmunología y alergia. https://orcid.org/0000-0003-3548-0385

DOI:

https://doi.org/10.24265/horizmed.2025.v25n2.11

Keywords:

Interferon Type I , Granulomatous Disease, Chronic , Bone Marrow Transplantation

Abstract

We present the case of a male patient aged one year and six months, diagnosed with chronic
granulomatous disease since the first month of life, due to a mutation in the CYBB gene. Early
diagnosis was possible due to a family history of the same disease in an older brother aged 11
years and the detection of the mutation in the mother (carrier). The patient had a history of two
hospitalizations. The first lasted five months and was due to a diagnosis of community-acquired
pneumonia, complicated by respiratory failure, acute infectious diarrhea due to Pseudomonas
aeruginosa and cytomegalovirus infection. The second hospitalization occurred at 11 months of
age due to sepsis of gastrointestinal and respiratory origin.
The patient received antimicrobial prophylaxis with trimethoprim-sulfamethoxazole, itraconazole
and acyclovir, along with monthly intravenous immunoglobulin infusions, with limited response.
During the first hospitalization, at five months of age, a hematopoietic stem cell transplant was
attempted using his father as the donor; however, 0 % chimerism was achieved. Since October 2024 (at 12 months of age), subcutaneous interferon gamma therapy was initiated—representing the first reported case of its use in
Peru. Currently, six months after the initiation of interferon gamma therapy, the patient has not experienced any new infectious
episodes. Only three mild adverse reactions were reported following 98 doses. This case demonstrates the clinical utility and
safety of interferon gamma in individuals with chronic granulomatous disease. Patients who, for various reasons, are unable to
access definitive bone marrow transplantation may receive it in combination with standard antimicrobial prophylaxis.

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Published

2025-06-28

How to Cite

1.
Ruiz P, Alegre Yataco PS, Rivera Castillo FR, Aldave Becerra JC. Use of interferon gamma following prrimary graft failure after hematopoietic stem cell transplantation in a patient with chronic granulomatous disease in a public hospital in Peru: a case report. Horiz Med [Internet]. 2025Jun.28 [cited 2025Jun.29];25(2):e2884. Available from: https://pglt.aulavirtualusmp.pe/index.php/horizontemed/article/view/2884

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Case report