Characterization of a murine anti-laminin-1 monoclonal antibody (AK8) produced by immunization with mouse-derived laminin-1
2005

Study of a Mouse Antibody Against Laminin-1

Sample size: 10 publication 15 minutes Evidence: moderate

Author Information

Author(s): Akane Kondo, Junko Inagaki, Kazuko Kobayashi, Hideo Tsukamoto, Daisuke Yamamoto, Mikiya Nakatsuka, Nobuharu Suzuki, Motoyoshi Nomizu, Satoshi Amano, Hidehiko Matsubayashi, Tatsuji Yasuda, Luis R. Lopez, Yehuda Shoenfeld, Tsunehisa Makino, Eiji Matsuura

Primary Institution: Okayama University Graduate School of Medicine and Dentistry

Hypothesis

Autoantibodies against laminin-1 may directly affect the development and differentiation of basement membranes in placenta and/or embryos.

Conclusion

The AK8 monoclonal antibody specifically recognizes a structure in the G domain of laminin-a1 and may be useful for developing a mouse model for autoimmune-mediated fetal loss.

Supporting Evidence

  • AK8 mAb was established after ten independent cell fusions of splenocytes from immunized mice.
  • Immunostaining showed AK8 mAb recognized basement membranes in both mouse and human endometrial tissues.
  • AK8 mAb specifically bound to mouse laminin-1 and not to other laminin isoforms.

Takeaway

Scientists created a special mouse antibody that can help understand why some pregnancies fail. This antibody works on a part of a protein important for pregnancy.

Methodology

Mice were immunized with laminin-1, and hybridomas were created to produce the AK8 monoclonal antibody, which was then characterized using ELISA and Western blot techniques.

Limitations

The study may not fully represent human responses due to species differences.

Participant Demographics

Balb/c mice were used for immunization.

Digital Object Identifier (DOI)

10.1080/17402520400014168

Want to read the original?

Access the complete publication on the publisher's website

View Original Publication