Pathophysiologie der Peritonitis
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  • 作者:Dr. K. Beyer ; Dr. P. Menges ; Dr. W. Keßler ; Prof. Dr. C.-D. Heidecke
  • 关键词:Peritonitis ; Sepsis ; Inflammation ; Apoptosis ; Immunosuppression
  • 刊名:Der Chirurg
  • 出版年:2016
  • 出版时间:January 2016
  • 年:2016
  • 卷:87
  • 期:1
  • 页码:5-12
  • 全文大小:708 KB
  • 参考文献:1.Abu-Hijleh MF, Habbal OA, Moqattash ST (1995) The role of the diaphragm in lymphatic absorption from the peritoneal cavity. J Anat 186(Pt 3):453–467PubMed PubMedCentral
    2.Beyer K, Poetschke C, Partecke LI et al (2014) TRAIL induces neutrophil apoptosis and dampens sepsis-induced organ injury in murine colon ascendens stent peritonitis. PLoS One 9:e97451PubMed PubMedCentral CrossRef
    3.Broche F, Tellado JM (2001) Defense mechanisms of the peritoneal cavity. Curr Opin Crit Care 7:105–116PubMed CrossRef
    4.Busse M, Traeger T, Potschke C et al (2008) Detrimental role for CD4 + T lymphocytes in murine diffuse peritonitis due to inhibition of local bacterial elimination. Gut 57:188–195PubMed CrossRef
    5.Chen P, Stanojcic M, Jeschke MG (2014) Differences between murine and human sepsis. Surg Clin North Am 94:1135–1149PubMed CrossRef
    6.Cziupka K, Busemann A, Partecke LI et al (2010) Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) improves the innate immune response and enhances survival in murine polymicrobial sepsis. Crit Care Med 38:2169–2174PubMed CrossRef
    7.Davey MS, Lin CY, Roberts GW et al (2011) Human neutrophil clearance of bacterial pathogens triggers anti-microbial gammadelta T cell responses in early infection. PLoS Pathog 7:e1002040PubMed PubMedCentral CrossRef
    8.Geissmann F, Jung S, Littman DR (2003) Blood monocytes consist of two principal subsets with distinct migratory properties. Immunity 19:71–82PubMed CrossRef
    9.Glik A, Douvdevani A (2006) T lymphocytes: the „cellular“ arm of acquired immunity in the peritoneum. Perit Dial Int 26:438–448PubMed
    10.Heel KA, Hall JC (1996) Peritoneal defences and peritoneum-associated lymphoid tissue. Br J Surg 83:1031–1036PubMed CrossRef
    11.Hotchkiss RS, Monneret G, Payen D (2013) Sepsis-induced immunosuppression: from cellular dysfunctions to immunotherapy. Nat Rev Immunol 13:862–874PubMed PubMedCentral CrossRef
    12.Italiani P, Boraschi D (2014) From Monocytes to M1/M2 Macrophages: phenotypical vs. Functional Differentiation. Front Immunol 5:514PubMed PubMedCentral CrossRef
    13.Johnson CC, Baldessarre J, Levison ME (1997) Peritonitis: update on pathophysiology, clinical manifestations, and management. Clin Infect Dis 24:1035–1045, quiz 1046–1037PubMed CrossRef
    14.Kasten KR, Tschop J, Adediran SG et al (2010) T cells are potent early mediators of the host response to sepsis. Shock 34:327–336PubMed CrossRef
    15.Laurin LP, Brissette MJ, Lepage S et al (2012) Regulation of experimental peritonitis: a complex orchestration. Nephron Exp Nephrol 120:e41–e46PubMed CrossRef
    16.Lopez N, Kobayashi L, Coimbra R (2011) A Comprehensive review of abdominal infections. World J Emerg Surg 6:7PubMed PubMedCentral CrossRef
    17.Maier S, Traeger T, Entleutner M et al (2004) Cecal ligation and puncture versus colon ascendens stent peritonitis: two distinct animal models for polymicrobial sepsis. Shock 21:505–511PubMed CrossRef
    18.Morita CT, Jin C, Sarikonda G et al (2007) Nonpeptide antigens, presentation mechanisms, and immunological memory of human Vgamma2Vdelta2 T cells: discriminating friend from foe through the recognition of prenyl pyrophosphate antigens. Immunol Rev 215:59–76PubMed CrossRef
    19.Norton JA (2001) Surgery: basic science and clinical evidence. Springer, New YorkCrossRef
    20.Novotny AR, Reim D, Assfalg V et al (2012) Mixed antagonist response and sepsis severity-dependent dysbalance of pro- and anti-inflammatory responses at the onset of postoperative sepsis. Immunobiology 217:616–621PubMed CrossRef
    21.Rittirsch D, Flierl MA, Ward PA (2008) Harmful molecular mechanisms in sepsis. Nat Rev Immunol 8:776–787PubMed PubMedCentral CrossRef
    22.Tai X, Van Laethem F, Pobezinsky L et al (2012) Basis of CTLA-4 function in regulatory and conventional CD4(+) T cells. Blood 119:5155–5163PubMed PubMedCentral CrossRef
    23.Van Till JW, Van Veen SQ, Van Ruler O et al (2007) The innate immune response to secondary peritonitis. Shock 28:504–517PubMed
    24.Yung S, Chan TM (2012) Pathophysiological changes to the peritoneal membrane during PD-related peritonitis: the role of mesothelial cells. Mediators Inflamm 2012:484167PubMed PubMedCentral CrossRef
  • 作者单位:Dr. K. Beyer (1)
    Dr. P. Menges (1)
    Dr. W. Keßler (1)
    Prof. Dr. C.-D. Heidecke (1)

    1. Klinik für Chirurgie, Viszeral-, Thorax- und Gefäßchirurgie, Universitätsmedizin Greifswald, Ferdinand-Sauerbruch-Straße, 17475, Greifswald, Deutschland
  • 刊物类别:Medicine
  • 刊物主题:Medicine & Public Health
    Surgery
    Cardiac Surgery
    Pediatric Surgery
    Plastic Surgery
    Traumatic Surgery
    Vascular Surgery
  • 出版者:Springer Berlin / Heidelberg
  • ISSN:1433-0385
文摘
Despite intensive research efforts peritonitis leading to subsequent sepsis remains associated with a high mortality. The initial effector cells are the locally residing cells of the peritoneum, such as mesothelial cells, mast cells, macrophages and lymphocytes. Through the secretion of chemokines, an influx of neutrophils initially takes place followed by monocytes. The latter can differentiate into inflammatory macrophages. The non-directed activity of neutrophilic granulocytes is limited by the induction of apoptotic programs. Through the breaching of cytokines, bacteria and microbial products into the circulation, a systemic reaction in the sense of systemic inflammatory response syndrome (SIRS) or sepsis arises. This is viewed as a concomitant derailing of inflammatory as well as anti-inflammatory responses, which leads to extensive apoptosis of lymphocytes. The presentation of apoptotic cells leads to a strong immunosuppression. Due to the coexistence of hyperinflammation and immunosuppression, exact knowledge of the current immune status of the patient is a prerequisite in the development of immunotherapies for the treatment of sepsis.

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