Oral Delivery of a Novel Recombinant Streptococcus mitis Vector Elicits Robust Vaccine Antigen-Specific Oral Mucosal and Systemic Antibody Responses and T Cell Tolerance

The pioneer human oral commensal bacterium Streptococcus mitis has unique biologic features that make it an attractive mucosal vaccine or therapeutic delivery vector. S. mitis is safe as a natural persistent colonizer of the mouth, throat and nasopharynx and the oral commensal bacterium is capable of inducing mucosal antibody responses. A recombinant S. mitis (rS. mitis) that stably expresses HIV envelope protein was generated and tested in the germ-free mouse model to evaluate the potential usefulness of this vector as a mucosal vaccine against HIV. Oral vaccination led to the efficient and persistent bacterial colonization of the mouth and the induction of both salivary and systemic antibody responses. Interestingly, persistently colonized animals developed antigen-specific systemic T cell tolerance. Based on these findings we propose the use of rS. mitis vaccine vector for the induction of mucosal antibodies that will prevent the penetration of the mucosa by pathogens such as HIV. Moreover, the first demonstration of rS. mitis having the ability to elicit T cell tolerance suggest the potential use of rS. mitis as an immunotherapeutic vector to treat inflammatory, allergic and autoimmune diseases.

[1]  David C. Gondek,et al.  A mucosal vaccine against Chlamydia trachomatis generates two waves of protective memory T cells , 2015, Science.

[2]  S. Tzipori,et al.  Commensal Streptococcus mitis is a unique vector for oral mucosal vaccination. , 2015, Microbes and infection.

[3]  D. Jarrossay,et al.  The Oral Commensal Streptococcus mitis Shows a Mixed Memory Th Cell Signature That Is Similar to and Cross-Reactive with Streptococcus pneumoniae , 2014, PloS one.

[4]  Guido Ferrari,et al.  Progress in HIV-1 vaccine development. , 2014, The Journal of allergy and clinical immunology.

[5]  B. Haynes,et al.  Advancing Toward HIV-1 Vaccine Efficacy through the Intersections of Immune Correlates , 2013, Vaccines.

[6]  A. Izzo,et al.  An unbiased peptide-wide discovery approach to select Mycobacterium tuberculosis antigens that target CD8+ T cell response during infection. , 2013, Vaccine.

[7]  C. Hsieh,et al.  T cell tolerance and immunity to commensal bacteria. , 2012, Current opinion in immunology.

[8]  J. Izard,et al.  The Human Oral Microbiome , 2010, Journal of bacteriology.

[9]  Michael G Hudgens,et al.  Maternal or infant antiretroviral drugs to reduce HIV-1 transmission. , 2010, The New England journal of medicine.

[10]  G. Grandi,et al.  Functional Characterization of a Newly Identified Group B Streptococcus Pullulanase Eliciting Antibodies Able to Prevent Alpha-Glucans Degradation , 2008, PloS one.

[11]  M. Sheridan,et al.  Antibody binding to Streptococcus mitis and Streptococcus oralis cell fractions. , 2008, Archives of oral biology.

[12]  B. Bensing,et al.  Glycine Residues in the Hydrophobic Core of the GspB Signal Sequence Route Export toward the Accessory Sec Pathway , 2007, Journal of bacteriology.

[13]  B. Haynes,et al.  Generation of CD8+ T-Cell Responses by a Recombinant Nonpathogenic Mycobacterium smegmatis Vaccine Vector Expressing Human Immunodeficiency Virus Type 1 Env , 2006, Journal of Virology.

[14]  J. A. Aas,et al.  Defining the Normal Bacterial Flora of the Oral Cavity , 2005, Journal of Clinical Microbiology.

[15]  S. Reed,et al.  Cloning of the Gene Encoding a Protective Mycobacterium tuberculosis Secreted Protein Detected In Vivo during the Initial Phases of the Infectious Process1 , 2005, The Journal of Immunology.

[16]  Qingsheng Li,et al.  Peak SIV replication in resting memory CD4+ T cells depletes gut lamina propria CD4+ T cells , 2005, Nature.

[17]  Mario Roederer,et al.  Massive infection and loss of memory CD4+ T cells in multiple tissues during acute SIV infection , 2005, Nature.

[18]  D. Price,et al.  CD4+ T Cell Depletion during all Stages of HIV Disease Occurs Predominantly in the Gastrointestinal Tract , 2004, The Journal of experimental medicine.

[19]  S. Haataja,et al.  Streptococcus pyogenes Glycoprotein-Binding Strepadhesin Activity Is Mediated by a Surface-Associated Carbohydrate-Degrading Enzyme, Pullulanase , 2003, Infection and Immunity.

[20]  H. Weiner Oral tolerance: immune mechanisms and the generation of Th3-type TGF-beta-secreting regulatory cells. , 2001, Microbes and infection.

[21]  C. Whitacre,et al.  T-cell activation and receptor downmodulation precede deletion induced by mucosally administered antigen. , 2000, The Journal of clinical investigation.

[22]  A. Khoruts,et al.  Direct evidence that functionally impaired CD4+ T cells persist in vivo following induction of peripheral tolerance. , 1998, Journal of immunology.

[23]  R P Johnson,et al.  Gastrointestinal tract as a major site of CD4+ T cell depletion and viral replication in SIV infection. , 1998, Science.

[24]  T. Barrett,et al.  Functional differentiation of T cells in the intestine of T cell receptor transgenic mice. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[25]  W. Strober,et al.  High dose oral tolerance in ovalbumin TCR-transgenic mice: systemic neutralization of IL-12 augments TGF-beta secretion and T cell apoptosis. , 1996, Journal of immunology.

[26]  M. Evans,et al.  Clonal diversity of Streptococcus mitis biovar 1 isolates from the oral cavity of human neonates , 1996, Clinical and diagnostic laboratory immunology.

[27]  N. Van Houten,et al.  Direct measurement of anergy of antigen-specific T cells following oral tolerance induction. , 1996, Journal of immunology.

[28]  H. Weiner,et al.  Different kinetic patterns of cytokine gene expression in vivo in orally tolerant mice , 1994, European journal of immunology.

[29]  H. Weiner,et al.  Regulatory T cell clones induced by oral tolerance: suppression of autoimmune encephalomyelitis. , 1994, Science.

[30]  J. van Houte,et al.  Oral streptococcal colonization of infants. , 1993, Oral microbiology and immunology.

[31]  M. Taubman,et al.  Salivary IgA antibody to oral streptococcal antigens in predentate infants. , 1990, Oral microbiology and immunology.

[32]  F. L. Macrina,et al.  Helper plasmid cloning in Streptococcus sanguis: cloning of a tetracycline resistance determinant from the Streptococcus mutans chromosome , 1982, Journal of bacteriology.

[33]  M. Kilian,et al.  Ecology and nature of immunoglobulin A1 protease-producing streptococci in the human oral cavity and pharynx , 1981, Infection and immunity.

[34]  R. Genco,et al.  Isolation of an enzyme from Streptococcus sanguis which specifically cleaves IgA. , 1974, Journal of immunology.

[35]  S. Socransky,et al.  ESTABLISHMENT OF HUMAN INDIGENOUS BACTERIA IN GERM-FREE MICE , 1964, Journal of bacteriology.

[36]  R. Monteiro,et al.  IgA, IgA receptors, and their anti-inflammatory properties. , 2014, Current topics in microbiology and immunology.

[37]  H. Weiner,et al.  Peripheral deletion of antigen-reactive T cells in oral tolerance , 1995, Nature.

[38]  M. Taubman,et al.  Ontogeny of immunity to oral microbiota in humans. , 1992, Critical reviews in oral biology and medicine : an official publication of the American Association of Oral Biologists.