CTLA4 binders
The present invention provides molecules, such as ISVDs and Nanobodies, that bind to CTLA4 or human serum albumin. These molecules have been engineered so as to reduce the incidence of binding by pre-existing antibodies in the bodies of a subject administered such a molecule. Methods for increasing immune response, treating cancer and/or treating an infectious disease with such molecules are provided.
1. A CTLA4 binder comprising an immunoglobulin single variable domain (ISVD) comprising the amino acid sequence:
XVQLVESGGGVVQPGGSLRLSCAASGGTFSFYGMGWFRQAPGKEREFVADIRTSAGRTYY ADSVKGRFTISRDNSKNTVYLQMNSLRPEDTALYYCAAEPSGISGWDYWGQGTLVTVSS (SEQ ID NO: 60) that binds to human CTLA4 at one or more of the following residues:
(SEQ ID NO: 118)
VRVTVL;
(SEQ ID NO: 119)
ADSQVTEVC;
and
(SEQ ID NO: 120)
CKVELMYPPPYYLG;
2. The CTLA4 binder of claim 1 fused to a half-life extender.
3. The CTLA4 binder of claim 2 , wherein the half-life extender is an ISVD that binds to human serum albumin.
4. The CTLA4 binder of claim 3 wherein the ISVD that binds to human serum albumin is ALB11002 having the amino acid sequence set forth in SEQ ID NO: 66.
5. The CTLA4 binder of claim 1 comprising:
an ISVD that binds to CTLA4 comprising the amino acid sequence set forth in SEQ ID NO: 60 wherein X is D or E;
a peptide linker;
an ISVD that binds to CTLA4 comprising the amino acid sequence set forth in SEQ ID NO: 60 wherein X is D or E;
a peptide linker;
a half-life extender; and, optionally,
a C-terminal extension alanine.
6. The CTLA4 binder of claim 1 comprising:
an ISVD that binds to CTLA4 comprising the amino acid sequence set forth in SEQ ID NO: 60 wherein X is D or E;
a peptide linker;
a half-life extender; and, optionally,
a C-terminal extension alanine.
7. The CTLA4 binder of claim 5 wherein the peptide linker comprises the amino acid sequence GGGGSGGGGSGGGGSGGGGSGGGGSGGGGSGGGGS (SEQ ID NO: 65).
8. A CTLA4 binder comprising an immunoglobulin single variable domain (ISVD) comprising the amino acid sequence:
(SEQ ID NO: 62)
DVQLVESGGGVVQPGGSLRLSCAASGGTFSFYGMGWFRQAPGKEREFVA
DIRTSAGRTYYADSVKGRFTISRDNSKNTVYLQMNSLRPEDTALYYCAA
EPSGISGWDYWGQGTLVTVSSGGGGSGGGGSGGGGSGGGGSGGGGSGGG
GSGGGGSEVQLVESGGGVVQPGGSLRLSCAASGGTFSFYGMGWFRQAPG
KEREFVADIRTSAGRTYYADSVKGRFTISRDNSKNTVYLQMNSLRPEDT
ALYYCAAEPSGISGWDYWGQGTLVTVSSGGGGSGGGGSGGGGSGGGGSG
GGGSGGGGSGGGGSEVQLVESGGGVVQPGNSLRLSCAASGFTFSSFGMS
WVRQAPGKGLEWVSSISGSGSDTLYADSVKGRFTISRDNAKTTLYLQMN
SLRPEDTALYYCTIGGSLSRSSQGTLVTVSSA
that binds to human CTLA4 at one or more of the following residues:
(SEQ ID NO: 118)
VRVTVL;
(SEQ ID NO: 119)
ADSQVTEVC;
and
(93-106 of SEQ ID NO: 120)
CKVELMYPPPYYLG.
9. A CTLA4 binder comprising an immunoglobulin single variable domain (ISVD) comprising the amino acid sequence:
(SEQ ID NO: 64)
DVQLVESGGGVVQPGGSLRLSCAASGGTFSFYGMGWFRQAPGKEREFVA
DIRTSAGRTYYADSVKGRFTISRDNSKNTVYLQMNSLRPEDTALYYCAA
EPSGISGWDYWGQGTLVTVSSGGGGSGGGGSGGGGSGGGGSGGGGSGGG
GSGGGGSEVQLVESGGGVVQPGNSLRLSCAASGFTFSSFGMSWVRQAPG
KGLEWVSSISGSGSDTLYADSVKGRFTISRDNAKTTLYLQMNSLRPEDT
ALYYCTIGGSLSRSSQGTLVTVSSA
that binds to human CTLA4 at one or more of the following residues:
(SEQ ID NO: 118)
VRVTVL;
(SEQ ID NO: 119)
ADSQVTEVC;
and
(SEQ ID NO: 120)
CKVELMYPPPYYLG.
10. The CTLA4 binder of claim 1 which is multivalent.
11. A binder that cross-blocks a CTLA4 binder of claim 1 from binding to human CTLA4.
12. An injection device or vessel that comprises the CTLA4 binder of claim 1 optionally in association with a further therapeutic agent.
13. A method for preventing CTLA4 from binding to CD80 or CD86 comprising contacting CTLA4 with the CTLA4 binder of claim 1 optionally in association with a further therapeutic agent.
14. A method for enhancing an immune response in the body of a subject comprising administering an effective amount of the CTLA4 binder of claim 1 to the subject optionally in association with a further therapeutic agent.