Skip to main content
Infection and Immunity logoLink to Infection and Immunity
. 1995 Aug;63(8):2931–2940. doi: 10.1128/iai.63.8.2931-2940.1995

Enhanced respiratory clearance of nontypeable Haemophilus influenzae following mucosal immunization with P6 in a rat model.

J M Kyd 1, M L Dunkley 1, A W Cripps 1
PMCID: PMC173399  PMID: 7622215

Abstract

Nontypeable Haemophilus influenzae (NTHi) is a common cause of infection of the respiratory tract in children and adults. The search for an effective vaccine against this pathogen has focused on components of the outer membrane, and peptidoglycan-associated lipoprotein P6 is among the proposed candidates. This study investigated the immunogenicity of P6 in a rat respiratory model. P6 was purified from two strains of NTHi, one capsule-deficient strain and an H. influenzae type b strain, and assessed for clearance of both homologous and heterologous bacterial strains following mucosal immunization. A protective immune response was determined by enhancement of pulmonary clearance of live bacteria and an increased rate of recruitment of phagocytic cells to the lungs. This was most effective when Peyer's patch immunization was accompanied by an intratracheal (IT) boost. However, the rate of bacterial clearance varied between strains, which suggests some differences in anti-P6 immunological defenses recognizing the expression of the highly conserved P6 lipoprotein on the bacterial surface in some strains. P6-specific antibodies in both serum and bronchoalveolar lavage fluid were cross-reactive and did not differ significantly in strain specificity, demonstrating that difference in clearance was unlikely due to differences in P6-specific antibody levels. Serum homologous and heterologous P6-antibody was bactericidal against NTHi even when enhanced clearance had not been observed. Peyer's patch immunization induced P6-specific CD4+ T-helper cell proliferation in lymphocytes isolated from the mesenteric lymph nodes. An IT boost increased the level of P6-specific antibodies in serum and bronchoalveolar lavage fluid, and P6-specific mesenteric node lymphocyte proliferation. Cells from rats immunized with P6 demonstrated proliferation following stimulation with P6 from nonhomologous strains; however, there was some variation in proliferative responses to P6 from different strains in lymphocytes isolated from animals immunized with killed bacteria. The increase in P6-specific antibodies and T-helper cell responses following an IT boost correlated with an increased rate of recruitment of phagocytic cells and enhanced bacterial clearance of both homologous and heterologous bacteria in the lungs. The data suggests that P6 has the potential to afford protection against pulmonary infection by NTHi following the induction of effective antigen-specific B- and T-cell responses in mucosal tissues.

Full Text

The Full Text of this article is available as a PDF (421.8 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Baker P. J. T cell regulation of the antibody response to bacterial polysaccharide antigens: an examination of some general characteristics and their implications. J Infect Dis. 1992 Jun;165 (Suppl 1):S44–S48. doi: 10.1093/infdis/165-supplement_1-s44. [DOI] [PubMed] [Google Scholar]
  2. Barenkamp S. J., Bodor F. F. Development of serum bactericidal activity following nontypable Haemophilus influenzae acute otitis media. Pediatr Infect Dis J. 1990 May;9(5):333–339. doi: 10.1097/00006454-199005000-00006. [DOI] [PubMed] [Google Scholar]
  3. Barenkamp S. J., Granoff D. M., Munson R. S., Jr Outer-membrane protein subtypes of Haemophilus influenzae type b and spread of disease in day-care centers. J Infect Dis. 1981 Sep;144(3):210–217. doi: 10.1093/infdis/144.3.210. [DOI] [PubMed] [Google Scholar]
  4. Brandtzaeg P. Overview of the mucosal immune system. Curr Top Microbiol Immunol. 1989;146:13–25. doi: 10.1007/978-3-642-74529-4_2. [DOI] [PubMed] [Google Scholar]
  5. Cripps A. W., Dunkley M. L., Clancy R. L. Mucosal and systemic immunizations with killed Pseudomonas aeruginosa protect against acute respiratory infection in rats. Infect Immun. 1994 Apr;62(4):1427–1436. doi: 10.1128/iai.62.4.1427-1436.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Cripps A. W., Taylor D. C., Wallace F. J., Clancy R. L. Respiratory immunity stimulated by intestinal immunization with purified nontypeable Haemophilus influenzae antigens. J Infect Dis. 1992 Jun;165 (Suppl 1):S199–S201. doi: 10.1093/infdis/165-supplement_1-s199. [DOI] [PubMed] [Google Scholar]
  7. Cundell D. R., Taylor G. W., Kanthakumar K., Wilks M., Tabaqchali S., Dorey E., Devalia J. L., Roberts D. E., Davies R. J., Wilson R. Inhibition of human neutrophil migration in vitro by low-molecular-mass products of nontypeable Haemophilus influenzae. Infect Immun. 1993 Jun;61(6):2419–2424. doi: 10.1128/iai.61.6.2419-2424.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Deich R. A., Anilionis A., Fulginiti J., Metcalf B. J., Quataert S., Quinn-Dey T., Zlotnick G. W., Green B. A. Antigenic conservation of the 15,000-dalton outer membrane lipoprotein PCP of Haemophilus influenzae and biologic activity of anti-PCP antisera. Infect Immun. 1990 Oct;58(10):3388–3393. doi: 10.1128/iai.58.10.3388-3393.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Dunkley M. L., Clancy R. L., Cripps A. W. A role for CD4+ T cells from orally immunized rats in enhanced clearance of Pseudomonas aeruginosa from the lung. Immunology. 1994 Nov;83(3):362–369. [PMC free article] [PubMed] [Google Scholar]
  10. Dunkley M. L., Husband A. J. Routes of priming and challenge for IgA antibody-containing cell responses in the intestine. Immunol Lett. 1990 Nov;26(2):165–170. doi: 10.1016/0165-2478(90)90140-l. [DOI] [PubMed] [Google Scholar]
  11. Dunkley M. L., Husband A. J. The induction and migration of antigen-specific helper cells for IgA responses in the intestine. Immunology. 1986 Mar;57(3):379–385. [PMC free article] [PubMed] [Google Scholar]
  12. Green B. A., Metcalf B. J., Quinn-Dey T., Kirkley D. H., Quataert S. A., Deich R. A. A recombinant non-fatty acylated form of the Hi-PAL (P6) protein of Haemophilus influenzae elicits biologically active antibody against both nontypeable and type b H. influenzae. Infect Immun. 1990 Oct;58(10):3272–3278. doi: 10.1128/iai.58.10.3272-3278.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Green B. A., Quinn-Dey T., Zlotnick G. W. Biologic activities of antibody to a peptidoglycan-associated lipoprotein of Haemophilus influenzae against multiple clinical isolates of H. influenzae type b. Infect Immun. 1987 Dec;55(12):2878–2883. doi: 10.1128/iai.55.12.2878-2883.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Green B. A., Vazquez M. E., Zlotnick G. W., Quigley-Reape G., Swarts J. D., Green I., Cowell J. L., Bluestone C. D., Doyle W. J. Evaluation of mixtures of purified Haemophilus influenzae outer membrane proteins in protection against challenge with nontypeable H. influenzae in the chinchilla otitis media model. Infect Immun. 1993 May;61(5):1950–1957. doi: 10.1128/iai.61.5.1950-1957.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Groeneveld K., van Alphen L., Voorter C., Eijk P. P., Jansen H. M., Zanen H. C. Antigenic drift of Haemophilus influenzae in patients with chronic obstructive pulmonary disease. Infect Immun. 1989 Oct;57(10):3038–3044. doi: 10.1128/iai.57.10.3038-3044.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Harabuchi Y., Faden H., Yamanaka N., Duffy L., Wolf J., Krystofik D. Human milk secretory IgA antibody to nontypeable Haemophilus influenzae: possible protective effects against nasopharyngeal colonization. J Pediatr. 1994 Feb;124(2):193–198. doi: 10.1016/s0022-3476(94)70302-7. [DOI] [PubMed] [Google Scholar]
  17. Kiyono H., Bienenstock J., McGhee J. R., Ernst P. B. The mucosal immune system: features of inductive and effector sites to consider in mucosal immunization and vaccine development. Reg Immunol. 1992 Mar-Apr;4(2):54–62. [PubMed] [Google Scholar]
  18. Kyd J. M., Taylor D., Cripps A. W. Conservation of immune responses to proteins isolated by preparative polyacrylamide gel electrophoresis from the outer membrane of nontypeable Haemophilus influenzae. Infect Immun. 1994 Dec;62(12):5652–5658. doi: 10.1128/iai.62.12.5652-5658.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
  20. Loeb M. R., Smith D. H. Outer membrane protein composition in disease isolates of Haemophilus influenzae: pathogenic and epidemiological implications. Infect Immun. 1980 Dec;30(3):709–717. doi: 10.1128/iai.30.3.709-717.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. McGhee J. R., Kiyono H. New perspectives in vaccine development: mucosal immunity to infections. Infect Agents Dis. 1993 Apr;2(2):55–73. [PubMed] [Google Scholar]
  22. McGhee J. R., Mestecky J., Dertzbaugh M. T., Eldridge J. H., Hirasawa M., Kiyono H. The mucosal immune system: from fundamental concepts to vaccine development. Vaccine. 1992;10(2):75–88. doi: 10.1016/0264-410x(92)90021-b. [DOI] [PubMed] [Google Scholar]
  23. Munson R. S., Jr, Granoff D. M. Purification and partial characterization of outer membrane proteins P5 and P6 from Haemophilus influenzae type b. Infect Immun. 1985 Sep;49(3):544–549. doi: 10.1128/iai.49.3.544-549.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Murphy T. F., Apicella M. A. Nontypable Haemophilus influenzae: a review of clinical aspects, surface antigens, and the human immune response to infection. Rev Infect Dis. 1987 Jan-Feb;9(1):1–15. doi: 10.1093/clinids/9.1.1. [DOI] [PubMed] [Google Scholar]
  25. Murphy T. F., Bartos L. C., Campagnari A. A., Nelson M. B., Apicella M. A. Antigenic characterization of the P6 protein of nontypable Haemophilus influenzae. Infect Immun. 1986 Dec;54(3):774–779. doi: 10.1128/iai.54.3.774-779.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Murphy T. F., Bartos L. C. Human bactericidal antibody response to outer membrane protein P2 of nontypeable Haemophilus influenzae. Infect Immun. 1988 Oct;56(10):2673–2679. doi: 10.1128/iai.56.10.2673-2679.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Murphy T. F., Bartos L. C. Purification and analysis with monoclonal antibodies of P2, the major outer membrane protein of nontypable Haemophilus influenzae. Infect Immun. 1988 May;56(5):1084–1089. doi: 10.1128/iai.56.5.1084-1089.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Murphy T. F., Bartos L. C., Rice P. A., Nelson M. B., Dudas K. C., Apicella M. A. Identification of a 16,600-dalton outer membrane protein on nontypeable Haemophilus influenzae as a target for human serum bactericidal antibody. J Clin Invest. 1986 Oct;78(4):1020–1027. doi: 10.1172/JCI112656. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Murphy T. F., Kirkham C., Sikkema D. J. Neonatal, urogenital isolates of biotype 4 nontypeable Haemophilus influenzae express a variant P6 outer membrane protein molecule. Infect Immun. 1992 May;60(5):2016–2022. doi: 10.1128/iai.60.5.2016-2022.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Musher D. M., Kubitschek K. R., Crennan J., Baughn R. E. Pneumonia and acute febrile tracheobronchitis due to haemophilus influenzae. Ann Intern Med. 1983 Oct;99(4):444–450. doi: 10.7326/0003-4819-99-4-444. [DOI] [PubMed] [Google Scholar]
  31. Nelson M. B., Apicella M. A., Murphy T. F., Vankeulen H., Spotila L. D., Rekosh D. Cloning and sequencing of Haemophilus influenzae outer membrane protein P6. Infect Immun. 1988 Jan;56(1):128–134. doi: 10.1128/iai.56.1.128-134.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Nelson M. B., Munson R. S., Jr, Apicella M. A., Sikkema D. J., Molleston J. P., Murphy T. F. Molecular conservation of the P6 outer membrane protein among strains of Haemophilus influenzae: analysis of antigenic determinants, gene sequences, and restriction fragment length polymorphisms. Infect Immun. 1991 Aug;59(8):2658–2663. doi: 10.1128/iai.59.8.2658-2663.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Nelson M. B., Murphy T. F., van Keulen H., Rekosh D., Apicella M. A. Studies on P6, an important outer-membrane protein antigen of Haemophilus influenzae. Rev Infect Dis. 1988 Jul-Aug;10 (Suppl 2):S331–S336. doi: 10.1093/cid/10.supplement_2.s331. [DOI] [PubMed] [Google Scholar]
  34. Sikkema D. J., Nelson M. B., Apicella M. A., Murphy T. F. Outer membrane protein P6 of Haemophilus influenzae binds to its own gene. Mol Microbiol. 1992 Feb;6(4):547–554. doi: 10.1111/j.1365-2958.1992.tb01499.x. [DOI] [PubMed] [Google Scholar]
  35. Suzuki H., Terada T. Removal of dodecyl sulfate from protein solution. Anal Biochem. 1988 Jul;172(1):259–263. doi: 10.1016/0003-2697(88)90440-x. [DOI] [PubMed] [Google Scholar]
  36. Toews G. B., Vial W. C., Hansen E. J. Role of C5 and recruited neutrophils in early clearance of nontypable Haemophilus influenzae from murine lungs. Infect Immun. 1985 Oct;50(1):207–212. doi: 10.1128/iai.50.1.207-212.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Troelstra A., Vogel L., van Alphen L., Eijk P., Jansen H., Dankert J. Opsonic antibodies to outer membrane protein P2 of nonencapsulated Haemophilus influenza are strain specific. Infect Immun. 1994 Mar;62(3):779–784. doi: 10.1128/iai.62.3.779-784.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Wallace F. J., Clancy R. L., Cripps A. W. An animal model demonstration of enhanced clearance of nontypable Haemophilus influenzae from the respiratory tract after antigen stimulation of gut-associated lymphoid tissue. Am Rev Respir Dis. 1989 Aug;140(2):311–316. doi: 10.1164/ajrccm/140.2.311. [DOI] [PubMed] [Google Scholar]
  39. Wallace F. J., Cripps A. W., Clancy R. L., Husband A. J., Witt C. S. A role for intestinal T lymphocytes in bronchus mucosal immunity. Immunology. 1991 Sep;74(1):68–73. [PMC free article] [PubMed] [Google Scholar]
  40. Wysocki L. J., Sato V. L. "Panning" for lymphocytes: a method for cell selection. Proc Natl Acad Sci U S A. 1978 Jun;75(6):2844–2848. doi: 10.1073/pnas.75.6.2844. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Xu-Amano J., Aicher W. K., Taguchi T., Kiyono H., McGhee J. R. Selective induction of Th2 cells in murine Peyer's patches by oral immunization. Int Immunol. 1992 Apr;4(4):433–445. doi: 10.1093/intimm/4.4.433. [DOI] [PubMed] [Google Scholar]
  42. Yamanaka N., Faden H. Local antibody response to P6 of nontypable Haemophilus influenzae in otitis-prone and normal children. Acta Otolaryngol. 1993 Jul;113(4):524–529. doi: 10.3109/00016489309135857. [DOI] [PubMed] [Google Scholar]
  43. Zlotnick G. W., Sanfilippo V. T., Mattler J. A., Kirkley D. H., Boykins R. A., Seid R. C., Jr Purification and characterization of a peptidoglycan-associated lipoprotein from Haemophilus influenzae. J Biol Chem. 1988 Jul 15;263(20):9790–9794. [PubMed] [Google Scholar]

Articles from Infection and Immunity are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES