Compositions and methods for inhibiting pathogen infection
The presently-disclosed subject matter relates to antibodies, compositions, and methods for inhibiting and treating virus infection in the respiratory tract and virus transmission through the respiratory tract. In particular, the presently-disclosed subject matter relates to inhibiting and treating virus infection in a subject using compositions and antibodies that trap viruses in mucus of the respiratory tract, thereby inhibiting transport of virus across or through mucus secretions.
1. A method for immobilizing or inhibiting a sexually transmitted infection by a pathogen, or reducing pathogen load in a subject in need thereof, the method comprising administering to a mucosal surface of the subject a recombinant antibody with a specific affinity for the pathogen, the recombinant antibody comprising a human or humanized Fc region, wherein the recombinant antibody comprises a population of antibodies in which at least 40% comprise an oligosaccharide having a GOF glycosylation pattern comprising a biantennary core glycan structure of Manα1-6(Manα1-3)Manβ1-4GlcNAcβ1-4GlcNAcβ1 with a fucose residue and a terminal N-acetylglucosamine, wherein the terminal N-acetylglucosamine is on each branch, that enhances the trapping potency of the recombinant antibody in mucus, so that the recombinant antibody binds to the pathogen to form an antibody/pathogen complex that is trapped in the subject's mucus.
2. The method of claim 1 , wherein the recombinant antibody comprises an N-linked glycosylation site on the Fc region of the antibodies to which the oligosaccharide is attached.
3. The method of claim 1 , wherein 50% or more of the recombinant antibodies in the population have a glycosylation pattern comprising the biantennary core glycan structure Manα1-6(Manα1-3)Manβ1-4GlcNAcβ1-4GlcNAcβ1 with the fucose and with the terminal N-acetylglucosamine on each branch.
4. The method of claim 1 , wherein the recombinant antibody is configured to bind to a non-neutralizing epitope of the pathogen.
5. The method of claim 1 , wherein administering comprises administering a dose at a sub-neutralization dose level.
6. The method of claim 1 , further comprising reducing the mobility of the pathogen in the patient's mucus to no more than about 50% relative to its mobility in water.
7. The method of claim 1 , further comprising reducing the percentage of pathogen that can penetrate the patient's mucus by at least 10%.
8. The method of claim 1 , wherein the recombinant antibody is a human or humanized IgG or IgM monoclonal antibody, or a fragment thereof.
9. The method of claim 1 , wherein the recombinant antibody is formulated as a topical composition.
10. The method of claim 1 , wherein the pathogen is selected from: Neisseria gonorrhoeae (gonorrhea); Chlamydia trachomatis ( chlamydia , lymphogranuloma venereum); Treponema pallidum (syphilis); Haemophilus ducreyi (chancroid); Klebsiella granulomatis or Calymmatobacterium granulomatis (donovanosis), Mycoplasma genitalium, Ureaplasma urealyticum (mycoplasmas); human immunodeficiency virus HIV-1 and HIV-2 (HIV, AIDS); HTLV-1 (T-lymphotrophic virus type 1); herpes simplex virus type 1 and type 2 (HSV-1 and HSV-2); Epstein-Barr virus; cytomegalovirus; human herpesvirus 6; varicella-zoster virus; human papillomaviruses (genital warts); hepatitis A virus, hepatitis B virus, hepatitis C virus (viral hepatitis); molluscum contagiosum virus (MCV); Trichomona vaginalis (trichomoniasis); and Candida albicans (vulvovaginal candidiasis).
11. The method of claim 1 , wherein the pathogen is herpes simplex virus type 1 or type 2.
12. A method of immobilizing a sexually transmitted pathogen in mucus of a subject's reproductive tract, the method comprising administering to the subject, via a topical route, a population of recombinant antibodies with a specific affinity for the pathogen, the recombinant antibodies comprising a human or humanized Fc region, wherein at least 40% of the recombinant antibodies comprise an oligosaccharide having a glycosylation pattern comprising the biantennary core glycan structure Manα1-6(Manα1-3)Manβ1-4GlcNAcβ1-4GlcNAcβ1 with a fucose and a terminal N-acetylglucosamine, wherein the terminal N-acetylglucosamine is on each branch to enhance the trapping potency of the recombinant antibody in mucus, so that the recombinant antibodies bind to the pathogen to form an antibody/pathogen complex that is trapped in the subject's mucus.
13. The method of claim 12 , wherein the recombinant antibodies are configured to bind to a non-neutralizing epitope of the pathogen.
14. The method of claim 12 , wherein administering comprises administering a dose at a sub-neutralization dose level.
15. The method of claim 12 , wherein the recombinant antibodies comprise N-linked glycosylation sites on the Fc region of the antibodies to which the oligosaccharide is attached.
16. The method of claim 12 , further comprising reducing the mobility of the pathogen to no more than about 50% relative to its mobility in water.
17. The method of claim 12 , further comprising reducing the percentage of pathogen that can penetrate mucus by at least 10%.
18. The method of claim 12 , wherein the recombinant antibody is a human or humanized IgG or IgM monoclonal antibody, or a fragment thereof.
19. The method of claim 12 , wherein the recombinant antibody is formulated as a gel, lotion, cream, or ointment.
20. The method of claim 12 , wherein at least 50% of the recombinant antibodies in the population have a glycosylation pattern comprising the biantennary core glycan structure Manα1-6(Manα1-3)Manβ1-4GlcNAcβ1-4GlcNAcβ1 with terminal N-acetylglucosamine on each branch.
21. The method of claim 12 , wherein the pathogen is selected from: Neisseria gonorrhoeae (gonorrhea); Chlamydia trachomatis ( chlamydia , lymphogranuloma venereum); Treponema pallidum (syphilis); Haemophilus ducreyi (chancroid); Klebsiella granulomatis or Calymmatobacterium granulomatis (donovanosis), Mycoplasma genitalium, Ureaplasma urealyticum (mycoplasmas); human immunodeficiency virus HIV-1 and HIV-2 (HIV, AIDS); HTLV-1 (T-lymphotrophic virus type 1); herpes simplex virus type 1 and type 2 (HSV-1 and HSV-2); Epstein-Barr virus; cytomegalovirus; human herpesvirus 6; varicella-zoster virus; human papillomaviruses (genital warts); hepatitis A virus, hepatitis B virus, hepatitis C virus (viral hepatitis); molluscum contagiosum virus (MCV); Trichomona vaginalis (trichomoniasis); and Candida albicans (vulvovaginal candidiasis).
22. The method of claim 12 , wherein the pathogen is herpes simplex virus type 1 or type 2.
23. A method for inhibiting a sexually transmitted pathogen in mucus of a subject's reproductive tract, the method comprising immobilizing the pathogen by administering to the subject a population of recombinant antibody in which at least 40% comprise an oligosaccharide having a GOF glycosylation pattern comprising a biantennary core glycan structure of Manα1-6(Manα1-3)Manβ1-→GlcNAcβ1-4GlcNAcβ1 with a fucose reside and a terminal N-acetylglucosamine, wherein the terminal N-acetylglucosamine is on each branch, wherein the recombinant antibody has a specific affinity for the pathogen so that the recombinant antibody is trapped in the subject's mucus, the recombinant antibody comprising a human or humanized Fc region, wherein the recombinant antibody comprises an oligosaccharide having a glycosylation pattern that enhances the trapping potency of the recombinant antibody in mucus.