Antiviral treatment comprising Blis containing probiotic products
This invention relates to methods of prophylactically or therapeutically treating viral infections particularly in the lower respiratory tract. Treatment of coronavirus infections is particularly contemplated. The invention also relates to the use of BLIS-producing Streptococcus strains, extracts and exudates thereof, and compositions containing same in the prevention, reduction, or treatment of such virus infections.
1 . A method for a prophylactic or therapeutic treatment of a lower respiratory tract (LRT) virus infection in a patient in need thereof, the method comprising administering to said patient an effective amount of a Blis product,
wherein the LRT virus is selected from the group consisting of influenza A, influenza B, respiratory syncytial virus (RSV), and coronavirus, and
wherein the Blis product is selected from the group consisting of S. salivarius strain K12 , S. salivarius strain M18 , S. salivarius strain DC0010A, S. salivarius strain Glasgow 3, exudates thereof, extracts thereof, and supernatants thereof.
2 . The method according to claim 1 , wherein the LRT virus is influenza A H1N1 or H3N2.
3 . The method according to claim 1 , wherein the LRT virus is influenza B Brisbane/60/2008.
4 . The method according to claim 1 , wherein the LRT virus is RSV A2.
5 . The method according to claim 1 , wherein the LRT virus is a coronavirus.
6 . The method according to claim 5 , wherein the coronavirus is a human coronavirus selected from the group consisting of SARS-CoV (2003), HCoV NL63 (2004), HKU1 (2005), MERS-CoV (2012), SARS-CoV-2 (2019), and variants thereof.
7 . The method according to claim 5 , wherein the coronavirus is SARS-CoV-2 (Covid-19) or a variant thereof.
8 . The method according to claim 1 , wherein the Blis product is in the form of a composition which further comprises a pharmaceutically acceptable diluent, carrier and/or excipient.
9 . The method according to claim 8 , wherein the composition is in the form of an inhalable composition, spray, nasal spray, lozenge, gum, capsule, powder, melt, food product, confectionary, or chewable.
10 . The method according to claim 8 , wherein the composition is in a form for administration via an inhaler, nebuliser, or atomiser.
11 . The method according to claim 8 , wherein the composition is in unit dosage form.
12 . The method according to claim 1 , wherein the method further comprises administering one or more other active agents.
13 . The method according to claim 12 , wherein the other active agent(s) are selected from the group consisting of antibodies, vaccines, immune modulators, probiotics, antimalarial compounds, antiviral compounds, antibiotic compounds, anti-inflammatory compounds and polymerase inhibitors.
14 . The method according to claim 13 , wherein the antimalarial compounds are selected from the group consisting of chloroquine and hydroxychloroquine.
15 . The method according to claim 13 , wherein the antiviral compounds are selected from the group consisting of lopinavir, ritonavir or a combination thereof.
16 . The method according to claim 13 , wherein the antibiotic compounds are selected from the group consisting of amikacin, amoxicillin, ampicillin, azithromycin, carbenicillin, cefotaxime, ceftazidime, ceftriaxone, cefuroxime, chloramphenicol, ciprofloxacin, clindamycin, dalacin, dalfopristin, daptomycin, doxycycline, enrofloxacin, ertapenem, erythromycin, gentamicin, marbofloxacin, meropenem, metronidazole, minocycline, moxifloxacin, nafcillin, ofloxacin, oxacillin, penicillin, quinupristin, rifampin, silver sulfadiazine, sulfamethoxazole, teicoplanin, tetracycline, tobramycin, trimethoprim, vancomycin, bacitracin, polymyxin B, and mixtures thereof.
17 . The method according to claim 1 wherein a high dose of S. salivarius is administered to said patient 1 to 4 times a day.
18 . The method according to claim 13 , wherein the anti-inflammatory compounds are selected from steroids, immunoglobulin, cytokine blockers, and JAK inhibitors.
19 . The method according to claim 13 , wherein the polymerase inhibitors are selected from remdesivir, galidesivir and favipiravir.
20 . The method according to claim 13 , wherein the antibodies are selected from bamlanivimab, casirivimab, etesevimab, VIR 7831, REGEN-COV and imdevimab, and combinations thereof.
21 . The method according to claim 13 , wherein the vaccines comprise a SARS CoV-2 vaccine.
22 . The method according to claim 13 , wherein the immune modulators are selected from budesonide (inhaled), AZD7422, azithromycin, doxycycline, tocilizumab, sarilumab, canakinumab, anakinra, baricitinib, ruxolitinib, acalabrutinib, brensocatib, ravulizumab, gemtuzumab ozogamicin, namilumab, infliximab, adalimumab, otilimab, Medi3506, leronlimab, risankizumab, lenzilumab, and IMU-838.