Conclusions
In writing this paper I have made an attempt, inadequate though it is, to seek explanations for some of the more puzzling manifestations of ophthalmic infections caused by TRIC agents. We have in the past possibly taken too naive a view of these syndromes, regarding features such as follicles and pannus purely from the viewpoint of a simple inflammatory process, and without giving enough consideration to the immunological mechanisms that may contribute to their causation. A quotation fromWilson andMiles' textbook (37) is apposite: “It is probable, indeed, that an increased sensitivity, associated with an increased vigour of response, is of frequent, perhaps almost of constant, occurrence at one stage or another of every infective disease, and that this sensitization plays a part in pathogenesis, particularly in subacute or chronic infections.”
The relative importance of humoral and of cellular factors in determining immunity to trachoma and the onset of healing is still not clear. Perhaps our thoughts on the immunopathology of PLT infections are still conditioned, even if subconsciously, by the erstwhile concept of the viral nature of these micro-organisms; and too much attention has been paid to the role of circulating antibody and not enough to that of cellular immunity. Nevertheless, the bacterial affinities of these agents, first pointed out byBedson andBland (1) and so admirably summarized byMoulder (23), lend plausibility to the idea that allergic reactions similar to those induced by bacteria may play an important role in pathogenesis.
In conclusion, it is apparent that my initial warning that I intended to provide more questions than answers has been amply fulfilled. My only justification is that some at least are open to experimental investigation; and although my colleagues and I cannot possibly tackle them all, we are now, we hope, working toward some of the solutions.
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References
Bedson, S. P., andJ. O. W. Bland: The developmental forms of psittacosis virus. Brit. J. exp. Path.15, 243 (1934).
Bernkopf, H., J. Orfila, andB. Maythar: Fluorescent antibodies in the fluid of the conjunctival sac of trachoma patients. Nature (Lond.)209, 725 (1966).
Bietti, G. B., P. Guerra, A. Felici, andR. Vozza: Research studies on trachoma. Acta Soc. Ophthal. Jap.66, 362 (1962).
Collier, L. H.: Experimental infection of baboons with inclusion blennorrhea and trachoma. Ann. N.T. Acad. Sci.98, 188 (1962).
Collier, L. H., andW. A. Blyth: Immunogenicity of experimental trachoma vaccines in baboons. I. Experimental methods and preliminary tests with vaeeines prepared in chick embryos and in HeLa cells. J. Hyg. (Lond.)64, 513 (1966).
Collier, L. H., andW. A. Blyth: Immunogenicity of experimental trachoma vaccines in baboons. II. Experiments with adjuvants and tests of cross protection. J. Hyg. (Lond.)64, 529 (1966).
Collier, L. H., W. A. Blyth, N. M. Larin, andJ. Treharne: Immunogenicity of experimental trachoma vaccines in baboons. III. Experiments with inactivated vaccines. J. Hyg. (Lond.)65, 79 (1967).
Collier, L. H., S. Duke-Elder, andB. R. Jones: Experimental trachoma produced by cultured virus. Part II. Brit. J. Ophthal.44, 65 (1960).
Conference on Trachoma andAllied Diseases. Amer. J. Ophthal. (in the press).
Dawson, C., E. Jawetz, P. Thygeson, andL. Hanna: Trachoma viruses isolated in the United States: 4. Infectivity and immunogenicity for monkeys. Proc. Soc. exp. Biol. (N.Y.)106, 898 (1961).
Freyche, M. J., andR. Nataf: Sur l'emploi de la cortisone comme test de guérison du trachome. Rev. int. Trachome29, 3 (1952).
Gear, J. H. S., F. B. Gordon, B. R. Jones, andS. D. Bell: Nomenclature of isolates of virus from trachoma and inclusion blennorrhea. Nature (Lond.)197, 26 (1963).
Gell, P. G. H., andIsobel T. Hinde: The histology of the tuberculin reaction and its modification by cortisone. Brit. J. exp. Path.32, 516 (1951).
Germuth, F. G., A. E. Maumenee, L. B. Senterfit, andA. D. Pollack: Immunohistologic studies on antigen-antibody reactions in the avascular cornea. I. Reactions in rabbits actively sensitized to foreign protein. J. exp. Med.115, 919 (1962).
Grayston, J. T.: Biology of the virus. In Symposium on Trachoma. Invest. Ophthal.2, 460 (1963).
Grayston, J. T., R. L. Woolridge, andS. P. Wang: Trachoma vaccine studies on Taiwan. Ann. N.Y. Acad. Sci.98, 352 (1962).
Halberstaedter, L., undS. von Prowazek: Über Zelleinschlüsse parasitärer Natur beim Trachom. Arb. Gesundh.-Amtl. (Berl.)26, 44 (1907).
Hurley, J. V., G. B. Ryan, andA. Friedman: The mononuclear response to intrapleural injection in the rat. J. Path. Bact.91, 575 (1966).
Jones, B. R.: Trachoma and allied infections. Trans. ophthal. Soc.81, 367 (1961).
Lassalle, Josette: Effet cytolytique de l'agent du. trachome et de l'agent de la conjonctivite à inclusions sur cultures de fibroblastes embryonnaires humains. C. R. Acad. Sci. (Paris)257, 2562 (1963).
Long, D. A., andA. A. Miles: Opposite actions of thyroid and adrenal hormones in allergic hypersensitivity. Lanceti, 492 (1950).
McCallan, A. F.: Trachoma. Butterworth & Co., London (1936).
Moulder, J. W.: The psittacosis group as bacteria. Ciba Lectures in Microbial Biochemistry. John Wiley and Sons Inc., New York (1964).
Nelken, E., I. C. Michaelson, D. Nelken, andJ. Gurevitch: Experimental corneal allergy: correlation between clinical and serologic findings. Amer. J. Ophthal.50, 583 (1960).
Nichols, R. L., andD. E. McComb: Immunofluorescent studies with trachoma and related antigens. J. Immunol.89, 545 (1962).
Ormsby, H. L., G. A. Thompson, G. G. Cousineau, L. A. Lloyd, andJ. Hassard: Topical therapy in inclusion conjunctivitis. Amer. J. Ophthal.35, 1811 (1952).
Reeve, P., andJanice Taverne: Some properties of the complement-fixing antigens of the agents of trachoma and inclusion blennorrhoea and the relationship of the antigens to the developmental cycle. J. gen. Microbiol.27, 501 (1962).
Sowa, S., J. Sowa, L. H. Collier, andW. A. Blyth: Trachoma and allied infections in a Gambian village. Spec. Rep. Ser. med. Res. Coun. (Lond.) No. 308 (1965).
Spector, W. G., andA. W. J. Lykke: The cellular evolution of inflammatory granulomata. J. Path. Bact.92, 163 (1966).
Spector, W. G., M. N.-I. Walters, andD. A. Willoughby: The origin of the mononuclear cells in inflammatory exudates induced by fibrinogen. J. Path. Bact.90, 181 (1965).
Tang, F. F., H. L. Chang, Y. T. Huang, andK. C. Wang: Studies on the etiology of trachoma with special reference to isolation of the virus in chick embryos. Chin. med. J.75, 429 (1957).
The Biology of the Trachoma Agent. Ann. N.Y. Acad. Sci.98, 1–382 (1962).
Thygeson, P.: Trachoma and inclusion conjunctivitis. In Viral and Rickettsial infections of man. J. B. Lippincott Company, Philadelphia, p. 365 (1948).
Thygeson, P.: Criteria of cure in trachoma with special reference to provocative tests. Rev. int. Trachome.30, 450 (1953).
Thygeson, P.: The cytologic diagnosis of trachoma. Rev. int. Trachome32, 421 (1955).
Wessely, K.: Über anaphylaktische Erscheinungen an der Hornhaut. (Experimentelle Erzeugung einer parenchymatösen Keratitis durch artfremdes Serum.) Münch. med. Wschr.58, 1713 (1911).
Wilson, G. S., andA. A. Miles: Topley and Wilson's Principles of Bacteriology and Immunity, 5th edition, Vol. II, p. 1430. Edward Arnold Ltd., London (1964).
World Health Organization: Wld Hlth Org. techn. Rep. Ser. No. 234 (1962).
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Dedicated to ProfessorJohn F. Enders on the occasion of his 70th birthday.
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Collier, L.H. The immunopathology of trachoma: Some facts and fancies. Archiv f Virusforschung 22, 280–293 (1967). https://doi.org/10.1007/BF01240523
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DOI: https://doi.org/10.1007/BF01240523