Brunner, H.

Fink, Edwin

Friesen, A.

Hofstetter, A.

Jochum, Marianne

Krause, W.

Rothauge, C. F.

Schießler, Hans

Schill, W.-B.

Weidner, W.

English

Open Access LMU

Chronic Prostatitis Clinical, Microbiological, Cytological and Immunological Aspects of Inflammation H . Brunner, Wuppertal W. Krause, Marburg C . F . Rothauge, Gießen W. Weidner, Gießen With 52 Figures and 59 Tables F. K. SCHATTAUER V E R L A G • STUTTGART - NEW Y O R K Edited by M ü n c h e n CIP-Kurztitelaufnahme der Deutschen Bibliothek Deutsche Bibliothek Cataloguing-in-Publication Data Chronic prostatitis : clin.. microbiolog.. cytolog. and immunolog. aspects of inflammation / ed. by H . Brunner . . . - Stuttgart ; New York : Schattauer, 1985. ISBN 3-7945-0978-1 NE: Brunner, Helmut [Hrsg.] The reproduction of general descriptive names, trade names, trade marks etc. in this publication, even when there is no special identification mark, is not to be taken as a sign that such names, as understood by the Trade Marks and Merchandise Marks Law, may accordingly be freely used by anyone. A l l rights reserved, no part of this book may be translated or reproduced in any form without written permission from Schattauer Verlag. © 1985 by F. K. Schattauer Verlag GmbH, Stuttgart, Germany Printed in Germany Composing, printing and binding: Allgäuer Zeitungsverlag GmbH, Kempten I S B N 3 - 7 9 4 5 - 0 9 7 8 - 1 Contents E. M . MEARES JR. Chronic Bacterial Prostatitis 1 N . J. BLACKLOCK Surgical Concepts in the Treatment of Chronic Bacterial Prostatitis . . 13 L. BAERT, J. MATTELAER, P. DE NOLLIN Treatment of Chronic Bacterial Prostatitis by Local Injection of Anti-biotics into Prostate 29 M . C. SHEPARD Role of Ureaplasma urealyticum in Male Lower Genital Tract Infec-tions 39 D. TAYLOR-ROBINSON, P. E. MUNDAY, N . F. H A N N A , B. J. THOMAS, P. H . FURR Microbiological Aspects of Non-Gonococcal Urethro-Prostatitis and its Probable Consequences 47 M . PEETERS, A . POLAK-VOGELZANG, F. DEBRUYNE, J. VAN DER VEEN Abacterial Prostatitis: Microbiological Data 55 H . BRUNNER, W. WEIDNER, H . G. SCHIEFER Studies on the Role of Ureaplasma urealyticum and Mycoplasma hominis in Prostatitis 63 H . G. SCHIEFER, W . WEIDNER, H . KRAUSS, U . GERHARDT, W . KRAUSE Prostatitis as Sequela of Non-Gonococcal Urethritis — A Prospective Study 75 H . KRAUSS, H . G. SCHIEFER, W. WEIDNER, M . ARENS, H . EBNER Significance of Chlamydia trachomatis in "Abacterial" Prostatitis . . . 85 G. M . COLPI, A . ZANOLLO, M . L. ROVEDA, A . TOMMASINI-DEGNA, G. BERETTA Bacterial Flora in Expressed Prostatic and Vesicular Secretions of In-fertile Subjects 93 T H . MERTENS, A . LANVERS, H . J. EGGERS Can Herpesvirus hominis be Isolated from the Genitourinary Tract of Men Having no Manifest Symptoms of Herpesvirus Infection? 101 V I I I Contents L . M . D. SHORTLIFFE, T. A. STAMEY The Immunologie Characterization of Bacterial Prostatitis Caused by Enterobacteriaceae 107 R . U . ANDERSON, S. H . M A Immunological Studies in Abacterial Prostatitis 113 R . U . ANDERSON Leukocyte Studies in Abacterial Prostatitis 121 E. JOHANNISSON, P. GRABER Cellular Changes in the Prostatic Massage Fluid and Prostatitis . . . . 125 W . L U D vi K The Diagnostic Significance of Leukocyte Counts in Prostatic Fluid . . 133 W . WEIDNER, H . EBNER Cytological Analysis of Urine After Prostatic Massage (VB3) — A New Technique for a Discriminating Diagnosis of Prostatitis 141 H . HOFMANN, H . BRUNNER, G. HAMMER, O. KURZ Clinical, Spermatological, and Microbiological Findings in Patients with Fertility Disorders and Chronic Prostatitis 153 H.-H. RIEDEL Leucocytospermia — A Sign for Chronic Infections of the Male Geni-tal Tract? 157 W . WEIDNER, W . KRAUSE, H . BRUNNER, H . G. SCHIEFER Semen Quality in Men with Urogenital Infections by Ureaplasma urealyticum 165 M . BALERNA, G. M . COLPI, A . CAMPANA, L. ROVED A, A. TOMMASINI-DEGNA, A . ZANOLLO Electrophoretical Analyses of Human Expressed Prostatic Secretion (EPS) and the Diagnosis of Prostatitis 173 H . W . BAUER, W . STURM, J. SCHÜLLER, E. SCHMIEDT Biochemical Analysis of Prostatic Fluid in Chronic Inflammation: pH, Immunoglobulins and Proteins 181 H . BLENK, A. HOFSTETTER The Behaviour of Complement C3 and other Serum Proteins in the Ejaculate in Chronic Prostatitis and their Diagnostic Importance . . . 189 A . S z i E G O L E i T , W . KRAUSE, H.-C. BECKER, W . WEIDNER Presence of Secretory- and Serum-IgA in Seminal Plasma 199 Contents I X H . G . SCHIEFER, W . WEIDNER, H . KRAUSS, U . GERHARDT, K . L. SCHMIDT Rheumatoid Factor-negative Arthritides and Urogenital Infections in Men 203 M. JOCHUM, W . - B . SCHILL, E. FINK, A . FRIESEN, A. HOFSTETTER, B . SCHIESSLER Proteinases and Proteinase Inhibitors in Ejaculates of Men with Adnex Affections 209 Dermatologische Klinik und Poliklinik der Universität München (Direktor: Prof. Dr. Dr. h. c. O. Braun-Falco) Abteilung für klinische. Chemie und klinische Biochemie (Direktor: Prof. Dr. H. Fritz) an der Chirurgischen Klinik der Universität München Urologische Abteilung des Stadt. Krankenhauses Thalkirchner Straße, München (Direktor: Prof Dr. A. Hofstetter) Proteinases and Proteinase Inhibitors in Ejaculates of Men with Adnex Affections M . JOCHUM, W.-B. SCHILL, E. FINK, A . FRIESEN, A . HOFSTETTER, H. SCHIESSLER Introduction Proteinases of the male genital tract are important primarily for the fertiliza-tion process. They are taking part also in coagulation and liquefaction of ejacu-late as well as in stimulation of sperm migration within the female genital secretions. Moreover, proteinases are involved as mediators of the inflamma-tory response in the male genital tract aggravating the clinical symptoms (SCHILL, 1975; HAFEZ, 1976; HAVEMANN and JANOFF, 1978). These proteinases are either sperm specific enzymes (acrosin), secretory products of the accessory sexual glands (seminin, BAEE-splitting enzyme, urokinase, tissue kallikrein) or they are liberated in the adnexal region during degranulation of leukocytes (elastase). In the male genital tract proteolytic activity of the proteinases are kept under control by potent antagonists, the high molecular weight plasma proteinase inhibitors a rproteinase inhibitor (formally (^-antitrypsin) and a rantichymo-trypsin as well as the low molecular weight, acid-stable secretory products leukostatin (HUSI-I) and acrostatin (HUSI-II) (SCHIESSLER etal . , 1976; SCHILL, 1976; SCHIESSLER and SCHILL, 1977; SCHILL and SCHIESSLER, 1977). We were interested, therefore, to see whether in chronic adnex affections alterations in the proteinase/proteinase inhibitor system of the ejaculate are measurable, probably qualified as diagnostic criteria. 210 M. Jochum et al. Material and methods Ejaculates were withdrawn from patients undergoing standard diagnostics such as 3-tube test and analysis of the urethral smear, prostatic fluid and urine. Diagnosis of chronic adnexitis was confirmed by the following criteria: signifi-cantly high numbers of gram-negative bacteria, enterococci, mycoplasmas, Ureaplasma urealyticum and Chlamydia trachomatis, leukocytes more than 20 per visual field; evidence of complement factor 3c and coeruloplasmin in semi-nal plasma. Ejaculates from 40 patients with adnex affections were exami-nated; 14 patients showed vegetative urogenital syndrome (VUG) and anogen-ital symptomcomplex (AGS), 24 patients suffered from chronic and 2 from acute adnexitis. Within the group of chronic adnexitis patients were further differenciated according to the concentration of the complement factor 3c as follows: patients with C3c values lower (n = 14) or higher (n = 10) than 1.2 mg%, respectively. Activities of seminin, urokinase, and the BAEE-split-ting enzyme in seminal plasma were determined using known methods (FRITZ, 1972; SCHILL, 1973). Tissue kallikrein was quantified by a specific radioim-munoassay (FINK and GÜTTL, 1978). The immunological concentrations of a r proteinase inhibitor, a rantichymotrypsin, acrostatin and leukostatin were measured by radial immunodiffusion ("Mancini-technique"). The concentra-tion of liberated granulocytic elastase bound to a rproteinase inhibitor (E-a^I ) was estimated by a newly developed enzyme-linked immunoassay (NEUMANN et al., 1983). Statistical evaluation was performed by the indepen-dent Student-t-test. Results and discussion Significance and physiological function of the BAEE-splitting enzyme from prostatic secretions is rather unknown. So far, only during viscosity disturb-ances of seminal plasma, a clearly lowered enzyme activity could be proven (SCHILL, personal communication). Seminin, originating also from prostata, is involved in clotting and liquefaction of sperm. Moreover, it may facilitate penetration of spermatozoa into cervix mucus. In contrast to normal ejacu-lates, both enzymes showed a significant decrease during chronic adnexitis as well in VUG as in AGS. This might be caused probably by massage of prostata before ejaculation. With acute adnexitis, a clear increase in enzyme-concen-trations was measurable in accordance with a commonly observed enhance-ment of organ function and synthesis during acute inflammatory reactions (Fig. 1). Proteinases and Proteinase Inhibitors in Ejaculates of Men with Adnex Affections 211 BAEE-Splitting Enzyme (BAEE/ADH-Test) 12CH 100-| 80i E 60-Ü0-20-100-I 80 5 * 60-1 40-20-Seminin (ATEE/ADH-Test) HP VUG+AGS CA. A.A. HP VUG+AGS C A . A.A. Fig. 1. Activity of BAEE-splitting enzyme and seminin in ejaculates of men with adnex affections (H.P. = healthy persons: V U G = vegetative urogenital syndrome; AGS = anogenital symptom complex; C. A . = chronic adnexitis with complement factor C3 < 1.2 mg% or > 1.2 mg% ? respec-tively; A . A . = acute adnexitis). Urokinase and tissue kallikrein were also demonstrable in prostatic secre-tion; their physiological relevance, however, ist still unknown. Probably, tissue kallikrein takes part in stimulation and maintenance of spermatozoon motility via liberation of pharmacologically highly active kinins from sperm plasma kininogen. In comparison to healthy persons, both enzymes showed a slight, though statistically not significant reduction in patients with chronic adnexitis and V U G ; again, in acute adnexitis an expected increase of the enzymes' concentrations was measurable (Fig. 2). The high molecular weight plasma proteinase inhibitors a rproteinase in-hibitor and a rantichymotrypsin, transudated from serum into seminal plasma, showed no significant alterations during V U G , AGS or chronic adnexitis, re-spectively. However, throughout acute adnexitis the well-known dramatic in-crease of the inhibitors' concentrations was demonstrable in seminal plasma. This enhancement may be due not only to a considerably increased synthesis of the inhibitors as acute phase proteins during the acute inflammatory response but also to a lowered blood-seminal plasma-barrier (Fig. 3). The acid-stable, low molecular weight proteinase inhibitor leukostatin syn-thesized in the vesicular glands is supposed to be the natural antagonist of leukocyte proteinases. It did not exhibit significant alterations. The same holds true for acrostatin (Fig. 4), the highly potent inhibitor of the penetration en-zyme acrosin which is localized in the acrosome of the spermatozoon. The low 212 M. Jochum et al. U O 120-1 KX) 80 60 40 20H Urokinase (Substrate S-2LU) HP VUG'AGS C A 300-KX) IL 80 H 60-20 Tissue -Kalllkrtin (RIA) A.A. HP VUG'AGS CA A A Fig. 2. Activity of urokinase and concentration of tissue kallikrein in ejaculates of men with adnex affections. 50-L0-' 30-20 io H CT E (Xi~ Proteinase Inhibitor (Mancini-Technique) Q O D HP VUG+AGS C.A. A.A. 20-15 10 0Ci • Antichymotrypsin (Mancini - Technique) H.P VUG'AGS C.A. A.A. Fig. 3. Concentrations of a rproteinase inhibitor and a rantichymotrypsin in ejaculates of men with adnex affections. Proteinases and Proteinase Inhibitors in Ejaculates of Men with Adnex Affections 213 250 200-1 E 150-XX) 50 Leukostotin (HUSI-I) (Mancini - Technique) 100 I 80-60 L0 20 Acrostatin (HUSI-II) (Mancini -Technique) HP VUG+AGS C A . H.P C A . Azoospermie Fig. \ . Concentrations of leukostatin and acrostatin in ejaculates of men with adnex affections. molecular weight, acid-stable acrostatin — synthesized in vesicular glands and epididymis — showed a clear reduction of the inhibitor concentration only in man with occlusive azoospermia (SCHILL and SCHIESSLER, 1977). Summarizing the given data, the proteinases and proteinase inhibitors de-scribed above did not turn out to be significant diagnostic parameters in chronic adnexitis, V U G and AGS, respectively. This is, however, different with leukocytic proteinases during these inflammatory processes. The biological function of leukocytic proteinases is the intracellular protein catabolism of wasted endogenous substances and the degradation of phagocy-tized invasive organisms. I f released extracellularly due to degranulation or disintegration of leukocytes, these proteinases may enhance tissue damage and activation of the inflammatory response. Of the leukocytic proteinases known so far, the neutral proteinase elastase from polymorphonuclear granulocytes deserves special interest because of its high amount within the granules as well as its nearly unlimited cleavage specificity. However, due to a relatively rapid reaction with a rproteinase inhibitor, the most important inhibitor of this en-zyme, granulocytic elastase liberated extracellularly is found nearly exclusively in an already inactivated form. With a highly sensitive enzyme-linked immunoassay about 180 ng complexed elastase (E-a r PI) per ml were found in ejaculates of 10 healthy persons. Patients with V U G and AGS showed a highly significant elevation up to x = 214 M. Jochum et al. 1100 ng/ml. In chronic adnexitis a similar increase (x = 1200 ng/ml) could be shown in seminal plasma containing C3c concentrations below 1.2 mg%, whereas C3 amounts above 1.2 mg% were combined with a further dramatic increase of complexed elastase up to 4500 ng/ml. Moreover, in acute adnexitis elastase levels far more than 10,000 ng/ml were measured (Fig. 5). From these preliminary results of 40 ejaculates, which of course will be confirmed with a more extended patient collective, we draw the following conclusions: 1. The levels of complexed granulocytic elastase proved to be a highly sensitive and qualified parameter of inflammatory processes in adnex affections. 2. Most of the biochemical parameters determined so far in ejaculates of pa-tients with adnex affections are only an indirect criterion of an impaired blood-seminal plasma-barrier during the inflammatory process. Levels of complexed granulocytic elastase, however, represent a direct quantificat on of an inflammatory mediator in the adnexial region. 3. Quantification of complexed elastase might become a reliable biochemical parameter additional to diagnostic criteria used now in adnex affections. This new parameter seems to reflect activity and seventy of an inflammatory process more specifically and offers, therefore, new aspects for controlling the course of the disease as well as the therapy. 20-i Complement Factor C3 (Mancini-Technique) 30-1 2 0-1.0-H.P • VUG•AGS O U C.A. Granulocytic Elastase (E-oqPI) Enzyme-linked immunoassay c A.A. • HP VUG+AGS C.A A.A Fig. 5. Concentrations of complement factor 3c and granulocytic elastase in complex with a, proteinase inhibitor (E-a,PI) in ejaculates of men with adnex affections. Proteinases and Proteinase Inhibitors in Ejaculates of Men with Adnex Affections 215 References ( 1 ) F INK, E., C. GÜTTL: Development of a radioimmunoassay for pig pancreatic kallikrein. J . Clin. Chem. Clin. Biochem. 16: 3 8 1 - 3 8 5 (1978) . ( 2 ) FRITZ, H . , M . ARNHOLD, B. FÖRG-BREY, L. J. D. ZANEVELD, G. F. B. SCHUMACHER: Verhal-ten der "Chymotrypsinähnlichen" Proteinase aus Humansperma gegenüber Protein-Protei-nase-Inhibitoren. Hoppe-Seylers Z . Physiol. Chem. 353: 1651 — 1653 (1972) . ( 3 ) HAFEZ, E. S. E. (ed.): Human Semen and Fertility Regulation in Men. Mosby, St. Louis 1976. ( 4 ) HAVEMANN, K . , A . JANOFF (eds.): Neutral Proteases of Human Polymorphonuclear Leuko-cytes. Urban & Schwarzenberg, Baltimore —Munich 1978. ( 5 ) NEUMANN, S., N . HENNRICH, G. GUNZER, H . LANG: Enzymelinked Immunoassay for com-plexes of Human Elastase with a,-Proteinase Inhibitor in Plasma. In: GOLDBERG, D. M . , M . WERNER (eds.): Progress in Clinical Enzymology I I , Masson Publ., New York 1983. ( 6 ) SCHIESSLER, H . , M . ARNHOLD, K . OHLSSON, H . FRITZ: Inhibitors of Acrosin and Granulo-cytes Proteinases from Human Genital Tract Secretions. Hoppe-Seyler's Z . Physiol. Chem. 357: 1 2 5 1 - 1 2 6 0 (1976) . ( 7 ) SCHIESSLER, H . , W.-B. SCHILL: Proteinaseinhibitoren in menschlichem Sperma: Biochemie und Biologische Funktion. Fortschr. d. Fertilitätsforschung 5: 189—191 (1977) . ( 8 ) SCHILL, W.-B.: Akrosin Activity in Human Spermatozoa: Methodological Investigations. Arch. Derm. Forsch. 248: 2 5 7 - 2 7 3 (1973) . ( 9 ) SCHILL, W.-B.: Quantitative Determination of High Molecular Weight Serum Proteinase Inhibitors in Human Semen. Andrologia 8: 359—364 (1976) . (10 ) SCHILL, W.-B.: Die Bedeutung proteolytischer Spermaenzyme für die Fertilität. Hautarzt 26: 5 1 4 - 5 2 3 (1975) . ( 1 1 ) SCHILL, W.-B., H . SCHIESSLER: Proteinaseinhibitoren in menschlichem Sperma: Quantitative Bestimmung und klinische Aspekte. Fortschritte der Fertilitätsforschung5: 192—194 (1977) . 

Akrosin Activity in Human Spermatozoa: Methodological Investigations.

Die Bedeutung proteolytischer Spermaenzyme für die Fertilität.

Enzymelinked Immunoassay for complexes of Human Elastase with a,-Proteinase Inhibitor

GÜTTL: Development of a radioimmunoassay for pig pancreatic kallikrein.

Inhibitors of Acrosin and Granulocytes Proteinases from Human Genital Tract Secretions. Hoppe-Seyler's Z.

Quantitative Determination of High Molecular Weight Serum Proteinase Inhibitors in Human Semen.

SCHIESSLER: Proteinaseinhibitoren in menschlichem Sperma: Quantitative Bestimmung und klinische Aspekte. Fortschritte der Fertilitätsforschung5:

SCHILL: Proteinaseinhibitoren in menschlichem Sperma: Biochemie und Biologische Funktion.

SCHUMACHER: Verhalten der &quot;Chymotrypsinähnlichen&quot; Proteinase aus Humansperma gegenüber Protein-Proteinase-Inhibitoren. Hoppe-Seylers Z.

Proteinases and proteinase inhibitors in ejaculates of men with adnex affections

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Proteinases and proteinase inhibitors in ejaculates of men with adnex affections

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