IP Library Granted Patent US 10,947,318
Granted Patent B2
US 10,947,318 · App. 15/698,816 · Granted Mar 16, 2021

IgE anti-HMW-MAA antibody

Inventors: Sophia Karagiannis (London, GB); Andrew Beavil (London, GB); Frank Nestle (London, GB)
Assignee: IGEM Therapeutics Limited
C07K16/3053A61K47/6865A61K2039/505C07K2317/24C07K2317/52C07K2317/732
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Quick Facts
Patent No.
US 10,947,318
App. No.
15/698,816
Granted
Mar 16, 2021
Kind
B2
Abstract

In one aspect, there is provided an antibody or a functional fragment thereof, wherein the antibody or functional fragment thereof is capable of binding specifically to high molecular weight melanoma associated antigen (HMW-MAA), and binding to an Fcε receptor.

Claims (22)

1. An IgE antibody, wherein the antibody is capable of:

(a) binding specifically to high molecular weight melanoma associated antigen (HMW-MAA); and

(b) binding to an Fcε receptor,

wherein the antibody comprises heavy chain CDR sequences of SEQ ID NO: 18, SEQ ID NO: 19 and SEQ ID NO: 20 and light chain CDR sequences of SEQ ID NO: 21, SEQ ID NO: 22 and SEQ ID NO: 23, and the heavy chain CDR sequence of SEQ ID NO:19 contains a conservative amino acid substitution of Asparagine (N) to Glutamine (Q).

2. The antibody of claim 1 , wherein the antibody comprises one or more constant regions capable of binding to an Fcε receptor.

3. The antibody of claim 1 , wherein the antibody has framework regions or constant domains that are derived from a mammalian species other than a mouse.

4. The antibody or functional fragment thereof of claim 3 , wherein the framework regions or constant domains are derived from a human.

5. The antibody of claim 1 , comprising one or more heavy chain constant domains selected from the group consisting of Cε1, Cε2, Cε3, and Cε4.

6. The antibody of claim 1 , wherein the antibody or functional fragment thereof comprises an ε heavy chain.

7. The antibody of claim 1 , wherein the antibody is conjugated to a detectable label, or a therapeutic agent, a cytotoxin, an encapsulating agent or a radioactive moiety.

8. The antibody of claim 1 , wherein the antibody comprises

(i) a VH domain comprising SEQ ID NO:4, and the VH domain contains a conservative amino acid substitution of Asparagine (N) to Glutamine (Q) in the heavy chain CDR sequence of SEQ ID NO: 19;

or

(ii) a VL domain comprising SEQ ID NO:6.

9. The antibody of claim 1 , wherein the antibody comprises

(i) a VH domain comprising SEQ ID NO:7, and the VH domain contains a conservative amino acid substitution of Asparagine (N) to Glutamine (Q) in the heavy chain CDR sequence of SEQ ID NO: 19;

or

(ii) a light chain comprising the amino acid sequence as defined in SEQ ID NO:8.

10. The antibody of claim 1 , wherein the conservative amino acid substitutions do not substantially affect or decrease affinity of the antibody to HMW-MAA and/or Fcε receptors.

11. The antibody of claim 1 , wherein the conservative amino acid substitution comprises exchange of Asparagine (N) to Glutamine (Q) at position 6 of SEQ ID NO:19.

12. A pharmaceutical composition comprising the antibody of claim 1 , and a pharmaceutically acceptable carrier.

13. A method of treating malignant melanoma in a subject, comprising administering to the subject a therapeutically effective amount of the pharmaceutical composition of claim 12 , wherein the malignant melanoma expresses HMW-MAA.

Assignments (1)
CHANGE OF NAME Recorded Oct 1, 2021
From: IGEM THERAPEUTICS LIMITED
To: EPSILOGEN LTD
Reel/Frame 057666/0805 →
Continuity (2)
Continuation 14348997
Related Publication 20180094074A1 · Apr 5, 2018