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Updated: Jul 1, 2026

Murine Model of Allergen Induced Asthma
Published on: May 14, 2012
Fermentation modifies camel-milk protein fractions (SDS-PAGE/SEC) and associates with lower IgE in an
Ahmad Al Athamneh1, Omar Al Haj1, Anas Khaleel2
1Department of Nutrition, Faculty of Pharmacy and Medical Sciences, University of Petra, Amman, Jordan.
Background:
Camel milk is widely consumed in regions with an increasing incidence of allergic diseases. Fermentation can reshape milk protein and peptide profiles, which may influence immunoreactivity.
Aim:
This study aimed to provide preliminary evidence on whether raw camel milk (RCM) and fermented camel milk (FCM) modulate allergic responses in an ovalbumin (OVA)-sensitized mouse model and to contextualize any in vivo effects with sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and size-exclusion chromatography (SEC) profiles.
Methods:
Female BALB/c mice (n = 21) were assigned to control (n = 6), sham (n = 5), raw camel milk (RCM; n = 5), or fermented camel milk (FCM; n = 5), sensitized, and challenged with ovalbumin. Clinical allergy scores and serum immunoglobulins were assessed (total IgE in all groups; OVA-specific IgE/IgA/IgG2a in sham, RCM, and FCM groups). Milk samples were subjected to SDS-PAGE and SEC.
Results:
Fermentation attenuated protein bands in the ~15-35 kDa region and shifted early SEC fractions relative to RCM. In vivo, total IgE differed across groups, driven primarily by lower values in non-sensitized controls; no BH-FDR-adjusted pairwise differences were detected between Sham and RCM/FCM. Antigen-specific immunoglobulins exhibited modest or non-significant changes; clinical scores were numerically lower but small in magnitude.
Conclusion:
Fermentation produced reproducible compositional shifts in camel milk, alongside group-level differences in total IgE that were primarily explained by non-sensitized controls rather than significant differences among sensitized groups. Although the effects on clinical scores and antigen-specific antibodies were limited in this small experiment, the data support further work integrating quantitative proteomics/peptidomics and cytokine profiling to clarify the mechanisms.

