Jurnal Medika Cendikia (e-Journal)
Vol 12 No 02 (2025): Jurnal Medika Cendikia

The Immunomodulatory Potential of Hesperidin from Garut Orange Peel (Citrus nobilis var. chrysocarpha) Against Human Metapneumovirus (HMPV) Infection: Based on In Vivo Mouse Model Study

sugiah, sugiah (Unknown)
Dadang Muhammad Hasyim, Dadang Muhammad Hasyim (Unknown)
Marsha Yulianti, Marsha Yulianti (Unknown)
Akbar Nurjamil, Akbar Nurjamil (Unknown)
N. Ai Erlinawati, N. Ai Erlinawati (Unknown)



Article Info

Publish Date
28 Nov 2025

Abstract

Acute respiratory infections (ARIs), including those caused by Human Metapneumovirus (HMPV), remain a global health concern, and no specific therapy or vaccine is currently available. Hesperidin, the main flavonoid in Garut orange peel (Citrus nobilis var. chrysocarpha), is known for its anti-inflammatory, antiviral, and immunomodulatory activities. This study was an in vivo pilot study using 35 male Balb/c mice divided into seven groups: normal control, negative control (5% imiquimod), positive control (levamisole), and hesperidin-treated groups at 50, 100, and 150 mg/kg body weight, either alone or in combination with imiquimod. Observed parameters included total leukocytes, lymphocytes, neutrophil-to-lymphocyte ratio (NLR), body weight, organ weight, and lung histology. Hesperidin was extracted using 70% ethanol and identified by thin-layer chromatography (TLC).Results showed that body weight data were normally distributed, with no significant differences between groups (p > 0.05), indicating that hesperidin was safe at the tested doses. Hematological analysis revealed significant differences in leukocyte counts (p = 0.001), lymphocytes (p = 0.002), and NLR (p = 0.001). Imiquimod induced systemic inflammation, as evidenced by increased leukocytes, lymphocytes, NLR, and lung inflammation scores. Hesperidin exhibited dose-dependent immunomodulatory effects; the 100 mg/kgBW dose combined with imiquimod produced the most optimal results, characterized by low NLR and a histology score of 0, reflecting controlled inflammation and effective adaptive immune activation. In contrast, the 150 mg/kgBW dose triggered excessive inflammatory responses.

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