Author/Authors :
Hosseinpour, Mitra 15 Khordad Hospital - ShahidBeheshti University of Medical Sciences, Tehran, Iran , Mashayekhi, Kazem Immuno-Biochemistry Lab - Immunology Research Center - Mashhad University of Medical Sciences, Mashhad, Iran , Falak, Reza Department of Immunology - School of Medicine - Iran University of Medical Sciences, Tehran, Iran , Jamalzehi, Sirous Department of Medical Laboratory Sciences - Iranshahr University of Medical Sciences, Iranshahr, Iran , Mohammadian Haftcheshmeh, Saeed Department of Medical Immunology - Nanotechnology Research Center - Bu-Ali Research Institute - School of Medicine - Mashhad University of Medical Sciences, Mashhad, Iran , Mousavi, Mohammad Javad Bushehr University of Medical Sciences, Bushehr, Iran , Soleimani, Anvar Department of Clinical Biochemistry - Faculty of Medicine - Mashhad University of Medical Sciences, Mashhad, Iran , Koushki, Khadijeh Immuno-Biochemistry Lab - Immunology Research Center - Mashhad University of Medical Sciences, Mashhad, Iran , Sankian, Mojtaba Immuno-Biochemistry Lab - Immunology Research Center - Mashhad University of Medical Sciences, Mashhad, Iran , Soukhtanloo, Mohammad Department of Clinical Biochemistry - Faculty of Medicine - Mashhad University of Medical Sciences, Mashhad, Iran
Abstract :
Allergy to non-specific lipidtransfer protein (nsLTP), the major allergen of grape (Vit v1), is
considered as one of the most common fruit allergies in Iran. Therefore, a specific monoclonal
antibody (mAb) can be used for the characterization and assessment of. Accordingly, this study aimed
to generate and characterize a mAb against Vit v1 with a diagnostic purpose.
To this end, Vit v1 allergen (9 kDa) was extracted using a modified Bjorksten extraction method.
Natural Vit v1-immunized mouse splenocytes were fused with SP2/0Ag-14 myeloma cells for
generating hybridoma cells. Specific antibody-secreting Hybridoma cells were selected using ELISA.
Finally, anti-Vit v1 mAb was characterized by western blotting, ELISA, and isotyping methods.
In the current study, a 9 kDa (Vit v1) protein was attained fromcrude and fresh juice of grape
extracts and the isotype of desired anti-Vit v1 mAb was determined as IgM with κ light chain. In
addition, The ELISA results demonstrated that anti-Vit v1 mAb was specified against natural Vit v1 in
the grape cultivar and related LTP allergens, such as Pla or 3 (p<0.0001).
In the present study, a specific mAb was produced for detecting the LTP allergen. This mAb with
a confirmed specificity can be utilized for evaluating the LTP allergens and their allergenicity in
different grape cultivars.
Keywords :
Non-specific lipid transfer protein , Monoclonal antibody , Lipid transfer protein , Grape , Allergy