Therapeutic peptides
The present disclosure provides, in part, compositions comprising peptides immuno specifically binds to defined binding partners, wherein the peptides comprise at least complementarity determining regions relating to the complementarity regions shown in Table 1.
1. An antibody or antigen binding fragment thereof that immunospecifically binds to MHC class I polypeptide-related sequence A (MICA), wherein the antibody or antigen binding fragment comprises
a heavy chain variable region (VH) CDR1 consists of the amino acid sequence shown in SEQ ID NO: 154, a VH CDR2 consists of the amino acid sequence shown in SEQ ID NO: 156, and a VH CDR3 consists of the amino acid sequence shown in SEQ ID NO: 158, and
a light chain variable region (VL) CDR1 consists of the amino acid sequence shown in SEQ ID NO: 161, a VL CDR2 consists of the amino acid sequence shown in SEQ ID NO: 163, a VL CDR3 consists of the amino acid sequence shown in SEQ ID NO: 165 and
a heterologous constant region or a heterologous Fc region.
2. The antibody or antigen binding fragment of claim 1 , comprising a VH region having the amino acid sequence shown in SEQ ID NO: 150; and a VL region having the amino acid sequence shown in SEQ ID NO: 152.
3. The antibody or antigen binding fragment of claim 1 , wherein the antibody or antigen binding fragment is human, humanized or chimeric.
4. A pharmaceutical composition comprising the antibody or antigen binding fragment of claim 1 .
5. The pharmaceutical composition of claim 4 , comprising one or more additional agents.
6. The antibody or antigen binding fragment of claim 1 , wherein the VH region comprises the amino acid sequence shown in SEQ ID NO: 150, or a variant thereof having 5 or fewer conservative amino acid substitutions in residues that are not within a CDR and wherein the VL region comprises the amino acid sequence shown in SEQ ID NO: 152, or a variant thereof having 5 or fewer conservative amino acid substitutions in residues that are not within a CDR.