IP Library Granted Patent US 9,738,688
Granted Patent B2
US 9,738,688 · App. 14/072,209 · Granted Aug 22, 2017

HIV-1 envelope glycoprotein

Inventors: Michael Caulfield (Fort Washington, PA); Albert Cupo (Stamford, CT); Hansi Dean (New York, NY); Simon Hoffenberg (Hartsdale, NY); C. Richter King (Washington, DC); P. J. Klasse (New York, NY); Andre Marozsan (Milford, CT); John P. Moore (New York, NY); Rogier W. Sanders (New York, NY); Andrew Ward (San Diego, CA); Ian Wilson (La Jolla, CA); Jean-Philippe Julien (San Diego, CA)
Assignees: INTERNATIONAL AIDS VACCINE INITIATIVE; THE SCRIPPS RESEARCH INSTITUTE; CORNELL UNIVERSITY
C07K14/005A61K39/12A61K39/21A61K39/39C12N2740/16034C12N2740/16122
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Quick Facts
Patent No.
US 9,738,688
App. No.
14/072,209
Granted
Aug 22, 2017
Kind
B2
Abstract

The present application relates to novel HIV-1 envelope glycoproteins, which may be utilized as HIV-1 vaccine immunogens, and antigens for crystallization, electron microscopy and other biophysical, biochemical and immunological studies for the identification of broad neutralizing antibodies. The present invention encompasses the preparation and purification of immunogenic compositions, which are formulated into the vaccines of the present invention.

Claims (32)

1. An engineered or non-naturally occurring HIV-1 envelope glycoprotein isolated from a BG505 virus and having a SOSIP mutation

wherein the glycoprotein is a BG505 SOSIP.664 gp140 trimer

and

wherein the SOSIP mutation comprises one or more mutations of the wild type amino acid alanine (A) or by wild type amino acid threonine (T) substitution with cysteine (C) (SOS mutation) and/or a mutation of the wild type amino acid isoleucine (I) by substitution with proline (P) (IP mutation);

wherein the BG505 SOSIP.664 gp140 trimer is more compact than a KNH1144 SOSIP.664G trimer isolated from with respect to envelope volume; and

wherein the BG505 SOSIP.664 gp140 trimer has a thermal denaturation midpoint (TM) of about 68 C.

2. An engineered or non-naturally occurring HIV-1 envelope glycoprotein isolated from a BG505 virus and having a SOSIP mutation, wherein the SOSIP mutation comprises a:

(a) mutation of the wild type amino acid threonine (T) by substitution with asparagine (N) to create 2G12, and PGT125, PGT126, PGT127, PGT128, PGT129, PGT130, and/or PGT 131 epitopes;

(b) mutation of the wild type amino acid isoleucine (I) by substitution with proline (P) to facilitation trimerization; or

(c) mutations of the wild type sequence REKR (SEQ ID NO: 1) at amino acid positions by substitution with RRRRRR (SEQ ID NO: 2) to enhance cleavage;

or any combination thereof.

3. An engineered or non-naturally occurring HIV-1 envelope comprising the amino acid sequence of SEQ ID NO: 3.

4. The glycoprotein of claim 1 , wherein the SOSIP mutation comprises a mutation of the wild type amino acid alanine (A) at position 498 of SEQ ID NO: 5 by substitution with cysteine (C) (SOS mutation).

5. The glycoprotein of claim 1 , wherein the SOSIP mutation comprises a mutation of the wild type amino acid threonine (T) at position 602 of SEQ ID NO: 5 by substitution with cysteine (C) (SOS mutation).

6. The glycoprotein of claim 1 , wherein the SOSIP mutation comprises a mutation of the wild type amino acid isoleucine (I) at position 556 of SEQ ID NO: 5 by substitution with proline (P) (IP mutation).

7. The glycoprotein of claim 1 ,

wherein the SOSIP mutation comprises a mutation of the wild type amino acid alanine (A) at position 498 of SEQ ID NO: 5 by substitution with cysteine (C) and of the wild type amino acid threonine (T) at position 602 of SEQ ID NO: 5 by substitution with cysteine (C) (SOS mutation) and a mutation of the wild type amino acid isoleucine (I) at position 556 of SEQ ID NO: 5 by substitution with proline (P) (IP mutation).

8. The glycoprotein of claim 2 , wherein the SOSIP mutation comprises a mutation of the wild type amino acid threonine (T) at position 330 of SEQ ID NO: 5 by substitution with asparagine (N).

9. The glycoprotein of claim 2 , wherein the SOSIP mutation comprises a mutation of the wild type amino acid isoleucine (I) at position 556 of SEQ ID NO: 5 by substitution with proline (P).

10. The glycoprotein of claim 2 , wherein the SOSIP mutation comprises mutations of the wild type sequence REKR (SEQ ID NO: 1) at amino acid positions 505-508 of SEQ ID NO: 5 by substitution with RRRRRR (SEQ ID NO: 2).

11. The glycoprotein of claim 2 , wherein the SOSIP mutation comprises a

(a) mutation of the wild type amino acid threonine (T) at position 330 of SEQ ID NO: 5 by substitution with asparagine (N);

(b) mutation of the wild type amino acid isoleucine (I) at position 556 of SEQ ID NO: 5 by substitution with proline (P); and

(c) mutations of the wild type sequence REKR (SEQ ID NO: 1) at amino acid positions 505-508 of SEQ ID NO: 5 by substitution with RRRRRR (SEQ ID NO: 2).

12. The glycoprotein of claim 3 consisting essentially of the amino acid sequence of SEQ ID NO: 3.

13. The glycoprotein of claim 3 consisting of the amino acid sequence of SEQ ID NO: 3.

14. A method of eliciting an immune response comprising administering to a mammal the glycoprotein of claim 1 .

15. The method of claim 14 further comprising an adjuvant.

16. The method of claim 15 wherein the adjuvant comprises alum.

17. A method of eliciting an immune response comprising administering to a mammal the glycoprotein of claim 3 .

18. The method of claim 17 further comprising an adjuvant.

19. The method of claim 18 wherein the adjuvant comprises alu

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 2, 2015
From: CAULFIELD, MICHAEL; DEAN, HANSI; HOFFENBERG, SIMON; KING, C. RICHTER
To: INTERNATIONAL AIDS VACCINE INITIATIVE
Reel/Frame 034863/0767 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 30, 2015
From: WARD, ANDREW; WILSON, IAN; JULIEN, JEAN-PHILIPPE
To: THE SCRIPPS RESEARCH INSTITUTE
Reel/Frame 034852/0291 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 30, 2015
From: CUPO, ALBERT; KLASSE, P. J.; MAROZSAN, ANDRE; MOORE, JOHN P.; SANDERS, ROGIER W.
To: CORNELL UNIVERSITY
Reel/Frame 034852/0421 →
CONFIRMATORY LICENSE Recorded Mar 12, 2014
From: CORNELL UNIVERSITY / CORNELL RESEARCH FOUNDATION, INC.
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 032436/0727 →
Continuity (2)
Provisional Application 61722739 · Nov 5, 2012
Related Publication 20140212458A1 · Jul 31, 2014