Development of diagnostic antibodies against immunoglobulin heavy chain variable region for heavy chain amyloidosis (AH amyloidosis). Issue 4 (13th March 2021)

• Record Type: Journal Article
• Authors: Nakagawa, Mayuko; Yazaki, Masahide; Kametani, Fuyuki; Katoh, Nagaaki; Yoshinaga, Tsuneaki; Higuchi, Keiichi; Sekijima, Yoshiki
• Is Part Of: Pathology international. Volume 71:Issue 4(2021)
• Page Start: 245
• Page End: 254
• Publication Date: 2021-03-13
• Subjects: AH amyloidosis -- diagnostic antibody -- immunoglobulin heavy chain -- immunohistochemistry -- variable region; Pathology -- Periodicals; 616.07
• DOI: 10.1111/pin.13081
• Languages: English
• ISSNs: 1320-5463

Abstract

Abstract : It is difficult to diagnose immunoglobulin heavy chain amyloidosis (AH amyloidosis) without proteomic analysis due to no useful diagnostic antibodies. The aim of this study was to develop diagnostic antibodies available to immunohistochemistry and immunoblotting. Two rabbit anti‐heavy chain variable region antibodies were generated and evaluated in immunohistochemical studies performed on 11 AH amyloidosis patients and 64 patients with other systemic amyloidoses. Additionally, immunoblotting was performed using extracted amyloid protein from one patient and serum samples from two patients with AH amyloidosis. Immunohistochemical analysis generated a positive outcome in 10 of 11 AH amyloidosis patients (sensitivity 90.9%). While positive staining was also observed in 9 of 64 non‐AH amyloidosis patients (specificity 85.9%), substitution of the blocking agent reversed the positive reactivity in 5 of 9 patients. Amyloid protein band was clearly detected via immunoblotting analysis, and protein bands with similar molecular weights of amyloid protein were observed in serum samples from patients with AH amyloidosis. The two antibodies may represent a powerful diagnostic tool for AH amyloidosis. In addition, our data revealed the existence of amyloidogenic variable region fragments in the serum of patients, suggesting their potential as diagnostic markers for AH amyloidosis.