A key feature of several anti-HIV neutralizing antibodies is the unusually long length of their CDR H3s. Cow antibodies are unique in having ultralong CDR3 regions that can be over 60 amino acids in length and are cysteine-rich. Crystal structures of two different antibody Fab fragments reveal that these CDR3s form a very unusual architecture composed of a long ?-strand stalk which supports a disulfide rich knob that protrudes far from the immunoglobulin surface. Interestingly, different antibodies contain different patterns of disulfides, which result in different knob structures. Deep sequencing reveals extensive diversity in the ultralong CDR3s where a multitude of different disulfides could potentially form within the knob. Analysis of clonally derived sequences suggests that this diversity results from somatic hypermutation of an ultralong germline D region that has a severe codon bias towards mutation to cysteine. Thus, the bovine antibody system may produce an unprecedented repertoire of mega CDR3s that fold into an impressive diversity of minifolds containing combinations of somatically generated disulfides. We have immunized cows using the BG505 gp140 trimer and found that they are capable of making a robust and broadly neutralizing serum antibody response. In this exploratory proposal, we will take advantage of the unusual ultralong cow antibody repertoire to generate new monoclonal antibodies against HIV gp120 with the goal of identifying new neutralizing epitopes on HIV.

Public Health Relevance

Many broadly neutralizing antibodies have CDR H3s that are unusually long. We have discovered the structure and diversity generating system of ultralong CDR H3 antibodies in cattle. We will generate new ultralong antibodies against gp120 to define new broadly neutralizing epitopes, which could lead to new strategies in designing HIV vaccines.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21AI120791-01A1
Application #
9141521
Study Section
HIV/AIDS Vaccines Study Study Section (VACC)
Program Officer
Shapiro, Stuart Z
Project Start
2016-02-01
Project End
2018-01-31
Budget Start
2016-02-01
Budget End
2017-01-31
Support Year
1
Fiscal Year
2016
Total Cost
Indirect Cost
Name
Scripps Research Institute
Department
Type
DUNS #
781613492
City
La Jolla
State
CA
Country
United States
Zip Code
92037
Stanfield, Robyn L; Haakenson, Jeremy; Deiss, Thaddeus C et al. (2018) The Unusual Genetics and Biochemistry of Bovine Immunoglobulins. Adv Immunol 137:135-164
Haakenson, Jeremy K; Huang, Ruiqi; Smider, Vaughn V (2018) Diversity in the Cow Ultralong CDR H3 Antibody Repertoire. Front Immunol 9:1262
Sok, Devin; Le, Khoa M; Vadnais, Melissa et al. (2017) Rapid elicitation of broadly neutralizing antibodies to HIV by immunization in cows. Nature 548:108-111