Treatment of inflammatory diseases with inhibitors of C5A activity
The present invention relates to inhibitors of C5a activity and their use in the treatment of cutaneous, neutrophilic, inflammatory diseases in a subject.
1. A method of treating a cutaneous, neutrophilic, inflammatory disease in a subject, the method comprising: administering to the subject in need thereof an effective amount of an agent that inhibits C5a activity in the subject, wherein the agent is an antibody or an antigen binding fragment thereof comprising
(i) a heavy chain CDR1 sequence of SEQ ID NO: 14, a heavy chain CDR2 sequence of SEQ ID NO: 10 and a heavy chain CDR3 sequence of SEQ ID NO: 6; and
(ii) a light chain CDR1 sequence of SEQ ID NO: 16, a light chain CDR2 sequence of SEQ ID NO: 12 and a light chain CDR3 sequence of SEQ ID NO: 8.
2. The method of claim 1 , wherein the agent exhibits one or more of the following properties:
the agent has a binding constant to C5a with a Kd value of 10 nM or less;
the agent inhibits binding between C5a and a C5a receptor; and
the agent exhibits at least 75% blocking activity for biological effects induced by one molecule C5a.
3. The method of claim 1 , wherein the cutaneous, neutrophilic, inflammatory disease is Hidradenitis suppurativa (HS) or a HS-related disease, wherein the HS-related disease is selected from the group consisting of Pyoderma gangrenosum (PG); PASH (PG, acne and Hidradenitis suppurativa); and PAPASH (Pyogenic arthritis, acne, PG and Hidradenitis suppurativa).
4. A method of inhibiting the interaction of a C5a receptor with C5a to treat Hidradenitis suppurativa (HS) or a HS-related disease in a subject, the method comprising administering to the subject an agent that inhibits C5a activity, wherein the agent is an antibody or an antigen binding fragment thereof comprising
(i) a heavy chain CDR1 sequence of SEQ ID NO: 14, a heavy chain CDR2 sequence of SEQ ID NO: 10 and a heavy chain CDR3 sequence of SEQ ID NO: 6; and
(ii) a light chain CDR1 sequence of SEQ ID NO: 16, a light chain CDR2 sequence of SEQ ID NO: 12 and a light chain CDR3 sequence of SEQ ID NO: 8,
thereby inhibiting the interaction of the C5a receptor with C5a and treating the disease, wherein the HS-related disease is selected from the group consisting of Pyoderma gangrenosum (PG); PASH (PG, acne and Hidradenitis suppurativa);
and PAP ASH (Pyogenic arthritis, acne, PG and Hidradenitis suppurativa); and wherein the agent exhibits at least 75% blocking activity for biological effects induced by one molecule C5a.
5. A method of treating Hidradenitis suppurativa (HS) or an HS-related disease in a subject, the method comprising: administering to the subject in need thereof an agent that inhibits C5a activity in the subject in an effective amount to treat HS or the HS-related disease, wherein the agent is an antibody or an antigen binding fragment thereof comprising:
(i) a heavy chain CDR1 sequence of SEQ ID NO: 14, a heavy chain CDR2 sequence of SEQ ID NO: 10 and a heavy chain CDR3 sequence of SEQ ID NO: 6; and
(ii) a light chain CDR1 sequence of SEQ ID NO: 16, a light chain CDR2 sequence of SEQ ID NO: 12 and a light chain CDR3 sequence of SEQ ID NO: 8;
wherein the HS-related disease is selected from the group consisting of Pyoderma gangrenosum (PG); PASH (PG, acne and Hidradenitis suppurativa); and PAP ASH (Pyogenic arthritis, acne, PG and Hidradenitis suppurativa); and wherein the agent exhibits at least 75% blocking activity for biological effects induced by one molecule C5a.
6. The method of claim 5 , wherein the antibody is IFX-1.
7. A method of treating Hidradenitis suppurativa (HS) or a HS-related disease in a subject, the method comprising: administering to a subject in need thereof an effective amount of IFX-1 antibody or an antigen binding fragment thereof, to treat HS or the HS-related disease, wherein the HS-related disease is selected from the group consisting of Pyoderma gangrenosum (PG); PASH (PG, acne and Hidradenitis suppurativa); and PAPASH (Pyogenic arthritis, acne, PG and Hidradenitis suppurativa).