Antibody fragments for the treatment of biofilm-related disorders
This disclosure provides antibody fragments and isolated polypeptides comprising the antibody fragments that are useful as a therapeutic for those with an existing infection characterized by the formation of biofilms. Antibody fragments and isolated polypeptides comprising the antibody fragments can be administered to detect, treat, or prevent infection and/or remediate biofilms. Bacteria that cannot form functional biofilms are more readily cleared by the remainder of the host's immune system and/or traditional antibiotics.
1. A method to disrupt a biofilm caused by biofilm-forming eubacteria in a subject in need thereof, one or more of: an inflammatory response; an infection; or a disease or condition, each associated with a biofilm forming eubacteria, wherein the eubacteria produce an integration host factor (IHF) DNABII protein in the subject, the method comprising administering to the subject an effective amount of a Fab fragment of an antibody comprising:
a)
i) a heavy chain (HC) variable region that comprises a complementarity determining region H1 (CDRH1) as set forth in SEQ ID NO: 112, a complementarity determining region H2 (CDRH2) as set forth in SEQ ID NO: 114, and a complementarity determining region H3 (CDRH3) as set forth in SEQ ID NO: 129; and
ii) a light chain (LC) variable region that comprises a complementarity determining region L1 (CDRL1) as set forth in SEQ ID NO: 131, a complementarity determining region L2 (CDRL2) as set forth in SEQ ID NO: 133, and a complementarity determining region L3 (CDRL3) as set forth in SEQ ID NO: 158; or
b)
i) a heavy chain (HC) variable region that comprises a complementarity determining region H1 (CDRH1) as set forth in SEQ ID NO: 113, a complementarity determining region H2 (CDRH2) as set forth in SEQ ID NO: 128, and a complementarity determining region H3 (CDRH3) as set forth in SEQ ID NO: 129; and
ii) a light chain (LC) variable region that comprises a complementarity determining region L1 (CDRL1) as set forth in SEQ ID NO: 132, a complementarity determining region L2 (CDRL2) as set forth in SEQ ID NO: 157, and a complementarity determining region L3 (CDRL3) as set forth in SEQ ID NOs: 159.
2. The method of claim 1 , wherein the Fab fragment further comprises a detectable label.
3. The method of claim 1 , further comprising administering an effective amount of an antibiotic and/or vaccine adjuvant.
4. The method of claim 1 , wherein the Fab fragment comprises
a heavy chain (HC) variable region that comprises a complementarity determining region H1 (CDRH1) as set forth in SEQ ID NO: 112, a complementarity determining region H2 (CDRH2) as set forth in SEQ ID NO: 114, and a complementarity determining region H3 (CDRH3) as set forth in SEQ ID NO: 129; and
a light chain (LC) variable region that comprises a complementarity determining region L1 (CDRL1) as set forth in SEQ ID NO: 131, a complementarity determining region L2 (CDRL2) as set forth in SEQ ID NO: 133, and a complementarity determining region L3 (CDRL3) as set forth in SEQ ID NO: 158.
5. The method of claim 1 , wherein the Fab fragment comprises an HC variable region as set forth in SEQ ID NO: 53 or an HC variable region having at least 90% sequence identity to SEQ ID NO: 53; and an LC variable region as set forth in SEQ ID NO: 57 or an LC variable region having at least 90% sequence identity to SEQ ID NO: 57.
6. The method of claim 1 , wherein the biofilm-forming eubacteria is selected from Aggregatibacter actinomycetemcomitans, Borrelia burgdorferi, Borrelia burgdorferi B31 , Bordetella pertussis, Bordetella pertussis Tohama I, Burkholderia pseudomallei, Burkholderia pseudomallei 668 , Burkholderia cenocepacia, Burkholderia cenocepacia HI2424 , Escherichia coli, Escherichia coli K12 MG1655, Haemophilus influenza, Haemophilus influenzae Rd KW20 , Haemophilus influenzae 86-028NP, Haemophilus influenzae R2866 , Haemophilus influenzae PittGG, Haemophilus influenzae PittEE, Haemophilus influenzae R2846 , Haemophilus influenzae 2019 , Helicobacter pylori, Helicobacter pylori 26695 , Klebsiella pneumoniae, Moraxella catarrhalis, Moraxella catarrhalis RH4, Neisseria gonorrhoeae, Neisseria gonorrhoeae FA1090 , Neisseria meningitidis, Neisseria meningitidis MC58, Pseudomonas aeruginosa, Prevotella intermedia, Prevotella intermedia 17, Aggregatibacter actinomycetemcomitans, Prevotella melaninogenica, Prevotella melaninogenica 25845, Salmonella enterica, Salmonella enterica typhi, Salmonella enterica CT18 , Treponema denticola, Treponema denticola 35405 , Treponema palladum, Treponema palladum Nichols, Vibrio cholera, Vibrio cholera El Tor, Vibrio cholera N16961 , Campylobacter spp., or Legionella pneumophila.
7. A method selected from: (1) a method for detecting the formation of a biofilm in a subject, (2) a method for monitoring the development or progression of a disease or a condition in a subject characterized by the formation of a biofilm, or (3) a method for monitoring the treatment of a disease or a condition in a subject characterized by the formation of a biofilm, wherein the biofilm is formed by a eubacteria that produces an integration host factor (IHF) or histone-like protein (HU) DNABII polypeptide, the method comprising administering an effective amount of a Fab fragment of an antibody, wherein detection of the antibody identifies the biofilm in the subject, the Fab fragment comprising:
a)
i) a heavy chain (HC) variable region that comprises a complementarity determining region H1 (CDRH1) as set forth in SEQ ID NO: 112, a complementarity determining region H2 (CDRH2) as set forth in SEQ ID NO: 114, and a complementarity determining region H3 (CDRH3) as set forth in SEQ ID NO: 129; and
ii) a light chain (LC) variable region that comprises a complementarity determining region L1 (CDRL1) as set forth in SEQ ID NO: 131, a complementarity determining region L2 (CDRL2) as set forth in SEQ ID NO: 133, and a complementarity determining region L3 (CDRL3) as set forth in SEQ ID NO: 158; or
b)
i) a heavy chain (HC) variable region that comprises a complementarity determining region H1 (CDRH1) as set forth in SEQ ID NO: 113, a complementarity determining region H2 (CDRH2) as set forth in SEQ ID NO: 128, and a complementarity determining region H3 (CDRH3) as set forth in SEQ ID NO: 129; and
ii) a light chain (LC) variable region that comprises a complementarity determining region L1 (CDRL1) as set forth in SEQ ID NO: 132, a complementarity determining region L2 (CDRL2) as set forth in SEQ ID NO: 157, and a complementarity determining region L3 (CDRL3) as set forth in SEQ ID NOs: 159 and
detecting said Fab fragment.
8. The method of claim 7 , further comprising administering to the subject an effective amount of an antibiotic and/or vaccine adjuvant.
9. The method of claim 7 , wherein the Fab fragment further comprises a detectable label.
10. The method of claim 7 , wherein the Fab fragment comprises
a heavy chain (HC) variable region that comprises a complementarity determining region H1 (CDRH1) as set forth in SEQ ID NO: 112, a complementarity determining region H2 (CDRH2) as set forth in SEQ ID NO: 114, and a complementarity determining region H3 (CDRH3) as set forth in SEQ ID NO: 129; and
a light chain (LC) variable region that comprises a complementarity determining region L1 (CDRL1) as set forth in SEQ ID NO: 131, a complementarity determining region L2 (CDRL2) as set forth in SEQ ID NO: 133, and a complementarity determining region L3 (CDRL3) as set forth in SEQ ID NO: 158.
11. The method of claim 7 , wherein the Fab fragment comprises an HC variable region as set forth in SEQ ID NO: 53 or an HC variable region having at least 90% sequence identity to SEQ ID NO: 53; and an LC variable region as set forth in SEQ ID NO: 57 or an LC variable region having at least 90% sequence identity to SEQ ID NO: 57.
12. The method of claim 7 , wherein the condition is selected from the group of: a chronic non-healing wound, a venous ulcer, a diabetic foot ulcer, an ear infection, a sinus infection, sinusitis, otitis, otitis media, bronchitis, a chronic obstructive pulmonary disease (COPD), an exacerbation of COPD, chronic cough, complications of or primary cause of cystic fibrosis (CF), cystic fibrosis, complications of or primary cause of community acquired pneumonia (CAP), CAP, a urinary tract infection, a recurrent urinary tract infection, a pulmonary infection, a lung infection of a cystic fibrosis patient, an infection of the gastrointestinal tract (GI), diarrhea, cholera, gall stones, gastric ulcers, an infection of the genital tract, dental caries, periodontitis, peri-implantitis, a periodontal disease, native valve infectious endocarditis, osteomyelitis, rhinosinusitis, prostatitis, abscesses, ‘staph’ infections, impetigo, secondary infection of burns, Lyme disease, an infection associated with implanted prostheses, an infected artificial device, an infected joint, a catheter-associated infection, an infected stent or other surgical implant.
13. The method of claim 7 , wherein the biofilm-forming eubacteria is selected from Aggregatibacter actinomycetemcomitans, Borrelia burgdorferi, Borrelia burgdorferi B31 , Bordetella pertussis, Bordetella pertussis Tohama I, Burkholderia pseudomallei, Burkholderia pseudomallei 668 , Burkholderia cenocepacia, Burkholderia cenocepacia HI2424 , Escherichia coli, Escherichia coli K12 MG1655 , Enterococcus faecalis, Enterococcus faecalis V583 , Haemophilus influenza, Haemophilus influenzae Rd KW20 , Haemophilus influenzae 86-028NP, Haemophilus influenzae R2866 , Haemophilus influenzae PittGG, Haemophilus influenzae PittEE, Haemophilus influenzae R2846 , Haemophilus influenzae 2019 , Helicobacter pylori, Helicobacter pylori 26695 , Klebsiella pneumoniae, Moraxella catarrhalis, Moraxella catarrhalis RH4, Neisseria gonorrhoeae, Neisseria gonorrhoeae FA1090 , Neisseria meningitidis, Neisseria meningitidis MC58, Pseudomonas aeruginosa, Prevotella intermedia, Prevotella intermedia 17, Aggregatibacter actinomycetemcomitans, Prevotella melaninogenica, Prevotella melaninogenica 25845 , Staphylococcus aureus, Staphylococcus aureus MW2 , Staphylococcus epidermidis, Staphylococcus epidermidis RP62A, Streptococcus agalactiae, Streptococcus agalactiae 2603 V/R, Streptococcus bovis, Streptococcus gallolyticus, Streptococcus gallolyticus UCN34 , Streptococcus gordonii, Streptococcus gordonii NCTC 7868 (Challis), Streptococcus mutans, Streptococcus mutans UA159 , Streptococcus pneumoniae, Streptococcus pneumoniae R6 , Streptococcus pyogenes, Streptococcus pyogenes MGAS 10270 , Streptococcus sobrinus, Streptococcus sobrinus 6715 , Salmonella enterica, Salmonella enterica typhi, Salmonella enterica CT18 , Treponema denticola, Treponema denticola 35405 , Treponema palladum, Treponema palladum Nichols, Vibrio cholera, Vibrio cholera El Tor, Vibrio cholera N16961 , Campylobacter spp., Legionella pneumophila , or Listeria monocytogenes.