HIV-1 Env fusion peptide nanoparticle carrier conjugates and their use

Patent metadata

Field	Value
Publication number	US-12053519-B2
Application number	US-201917277694-A
Country	US
Kind code	B2
Filing date	Sep 23, 2019
Priority date	Sep 23, 2018
Publication date	Aug 6, 2024
Grant date	Aug 6, 2024

Abstract

Embodiments of immunogenic conjugates including the HIV-1 Env fusion peptide and methods of their use and production are disclosed. In several embodiments, the immunogenic conjugates can be used to generate an immune response to HIV-1 Env in a subject, for example, to treat or prevent an HIV-1 infection in the subject.

First claim

It is claimed:

1. An immunogenic conjugate, comprising:
a self-assembling protein-nanoparticle carrier comprising a multimer of fusion proteins, wherein each fusion protein comprises a self-assembling protein nanoparticle subunit fused to a heterologous carrier protein, and wherein the fusion proteins self-assemble to form the self-assembling protein-nanoparticle carrier; and
HIV-1 Env fusion peptides conjugated to the self-assembling protein-nanoparticle carrier, wherein the HIV-1 Env fusion peptides comprise, from the N-terminus, the amino acid sequence of residue 512 to one of residues 514-521 of a human immunodeficiency virus type 1 (HIV-1) Envelope (Env) protein according to the HXB2 numbering system; and
wherein the immunogen elicits an immune response to HIV-1 Env.

2. A recombinant self-assembling nanoparticle subunit, comprising:
a lumazine synthase nanoparticle subunit comprising cysteine substitutions to introduce one or more non-native disulfide bonds to increase stability of the nanoparticle, wherein the cysteine substitutions comprise 121C and 131C substitutions, 121CG and 131C substitutions, 121GC and 131C substitutions, 7C and 40C substitutions, 3C and 50C substitutions, 82C and 131CG substitutions, 5C and 52C substitutions, or 95C and A101C substitutions, or a combination thereof, wherein residue numbering corresponds to a reference lumazine synthase subunit set forth as SEQ ID NO: 25;
an encapsulin nanoparticle subunit comprising cysteine substitutions to introduce one or more non-native disulfide bonds to increase stability of the nanoparticle, wherein the cysteine substitutions comprise 53C and 94C substitutions, 53C and 96C substitutions, or 146C and 185C substitutions, or a combination thereof, wherein residue numbering corresponds to a reference encapsulin subunit set forth as SEQ ID NO: 43;
an acinetobacter phage AP205 protein nanoparticle subunit comprising cysteine substitutions to introduce one or more non-native disulfide bonds to increase stability of the nanoparticle, wherein the cysteine substitutions comprise a T81C substitution, 53C and 100C substitution, or 82C and 80C substitutions, or a combination thereof, wherein residue numbering corresponds to a reference acinetobacter phage AP205 protein subunit set forth as SEQ ID NO: 316; or
a Hepatitis B capsid protein nanoparticle subunit comprising cysteine substitutions to introduce one or more non-native disulfide bonds to increase stability of the nanoparticle, wherein the cysteine substitutions comprise 25C and 127C substitutions, 14C and 36C substations, 29C and 127C substitutions, 18C and 36C substitutions, or 29C and 127C substitutions, or a combination thereof, wherein residue numbering corresponds to a reference Hepatitis B capsid protein subunit set forth as SEQ ID NO: 321.

3. A recombinant self-assembling nanoparticle subunit, comprising:
a ferritin nanoparticle subunit comprising or consisting of the amino acid sequence set forth as any one of SEQ ID NOs: 258-305;
a lumazine synthase nanoparticle subunit comprising or consisting of the amino acid sequence set forth as any one of SEQ ID NOs: 306-312;
an encapsulin nanoparticle subunit comprising or consisting of the amino acid sequence set forth as any one of SEQ ID NOs: 313-315;
a Acinetobacter phage AP205 protein nanoparticle subunit comprising or consisting of the amino acid sequence set forth as any one of SEQ ID NOs: 317-320; or
a Hepatitis B capsid protein nanoparticle subunit comprising or consisting of the amino acid sequence set forth as any one of SEQ ID NOs: 322-326.

4. The recombinant self-assembling nanoparticle subunit of claim 3 , wherein the recombinant self-assembling nanoparticle subunit is fused to a heterologous carrier protein.

5. The recombinant self-assembling nanoparticle subunit of claim 4 , wherein the heterologous carrier protein is selected from any one of a tetanus toxin heavy chain C fragment, a diphtheria toxin variant CRM197, and an H influenzae protein D, a Keyhole Limpet Hemocyanin (KLH) functional unit, a Meningococcal outer membrane protein complex protein, an Outer-membrane lipoprotein carrier protein, or a Cholera toxin B subunit.

6. The recombinant self-assembling nanoparticle subunit of claim 5 , wherein the heterologous carrier protein is the tetanus toxin heavy chain C fragment.

7. A nucleic acid molecule encoding the recombinant self-assembling nanoparticle subunit of claim 2 .

8. A recombinant self-assembling nanoparticle comprising the recombinant self-assembling nanoparticle subunit of claim 2 .

9. The recombinant self-assembling nanoparticle of claim 8 , conjugated to a vaccine antigen.

10. An immunogenic composition comprising the recombinant self-assembling nanoparticle of claim 9 .

11. A method for generating an immune response to a vaccine antigen in a subject, comprising administering to the subject an effective amount of the immunogenic composition of claim 10 to generate the immune response.

12. A nucleic acid molecule encoding the recombinant self-assembling nanoparticle subunit of claim 3 .

13. A recombinant self-assembling nanoparticle comprising the recombinant self-assembling nanoparticle subunit of claim 3 .

14. The recombinant self-assembling nanoparticle of claim 3 , conjugated to a vaccine antigen.

15. An immunogenic composition comprising the recombinant self-assembling nanoparticle of claim 14 .

16. A method for generating an immune response to a vaccine antigen in a subject, comprising administering to the subject an effective amount of the immunogenic composition of claim 15 to generate the immune response.

Assignees

• Us Health

Inventors

• Kwong Peter
• Ou Li
• Mascola John
• Zhang Baoshan
• Xu Kai
• Kong Wing-Pui
• Tsybovsky Yaroslav
• Chao Cara W
• Boyington Jeffrey
• Wang Yiran

Classifications

• A61K2039/645

  Dendrimers; Multiple antigen peptides · CPC title

• A61K2039/6081

  Albumin; Keyhole limpet haemocyanin [KLH] · CPC title

• A61K2039/6075

  Viral proteins · CPC title

• A61K2039/6068

  Other bacterial proteins, e.g. OMP · CPC title

• A61K2039/6037

  Bacterial toxins, e.g. diphteria toxoid [DT], tetanus toxoid [TT] · CPC title