Anti-baff nanobody and preparation and application thereof

By preparing and humanizing camel-derived chimeric anti-BAFF nanobodies, the shortcomings of existing BAFF monoclonal antibodies in the treatment of autoimmune diseases have been overcome. This has achieved effective blocking of the BAFF signaling pathway and disease inhibition, demonstrating excellent stability and therapeutic potential.

CN122404553APending Publication Date: 2026-07-17SHENYANG SUNSHINE PHARMA CO LTD
View PDF 0 Cites 0 Cited by

Patent Information

Authority / Receiving Office
CN · China
Patent Type
Applications(China)
Current Assignee / Owner
SHENYANG SUNSHINE PHARMA CO LTD
Filing Date
2025-01-15
Publication Date
2026-07-17

AI Technical Summary

Technical Problem

Existing BAFF monoclonal antibody drugs, such as Belimumab, still have unmet clinical needs in the treatment of autoimmune diseases such as systemic lupus erythematosus. There is a need to develop better anti-BAFF nanobodies to more effectively block the BAFF signaling pathway and inhibit its biological activity.

Method used

Camel-derived antibodies targeting BAFF were obtained by panning antibody libraries of immunized camels and phage display. Camel-derived chimeric anti-BAFF nanobodies were prepared by combining the Fc domain of IgG1 and then humanized to obtain humanized anti-BAFF nanobodies with better expression levels and biological activity.

Benefits of technology

It effectively blocks the BAFF signaling pathway, significantly inhibits BAFF-induced B cell activation and proliferation, and is superior to the existing drug Belimumab. It has excellent stability and clinical potential and is suitable for the treatment of a variety of autoimmune diseases.

✦ Generated by Eureka AI based on patent content.

Smart Images

  • Figure BDA0005244247070000101
    Figure BDA0005244247070000101
  • Figure BDA0005244247070000111
    Figure BDA0005244247070000111
  • Figure BDA0005244247070000121
    Figure BDA0005244247070000121
Patent Text Reader

Abstract

本发明提供了一种抗BAFF纳米抗体或其抗原结合片段,其重链可变区包含如SEQ ID NO:16所示的HCDR2以及SEQ ID NO:17或19所示的HCDR3。本发明的抗BAFF纳米抗体或其抗原结合片段可有效阻断BAFF信号通路,有效抑制BAFF的生物活性,可用于预防或治疗因BAFF所引起的B细胞活化、增殖或功能异常等导致的疾病。
Need to check novelty before this filing date? Find Prior Art