Literature DB >> 19325510

Secondary hemophagocytic lymphohistiocytosis and severe sepsis/ systemic inflammatory response syndrome/multiorgan dysfunction syndrome/macrophage activation syndrome share common intermediate phenotypes on a spectrum of inflammation.

Leticia Castillo1, Joseph Carcillo.   

Abstract

In an effort to attain earlier diagnoses in children with hemophagocytic lymphohistiocytosis (HLH), the International Histiocyte Society has now broadened their diagnostic criteria to no longer differentiate primary (HLH) and secondary hemophagocytic lymphohistiocytosis (SHLH). Five of the following eight diagnostic criteria needed to be met: 1) fever, 2) cytopenia of two lines, 3) hypertriglyceridemia and/or hypofibrinogenemia, 4) hyperferritinemia (>500 microg/L), 5) hemophagocytosis, 6) elevated soluble interleukin-2 receptor (CD25), 7) decreased natural killer-cell activity, and 8) splenomegaly can also commonly be found in patients with sepsis, systemic inflammatory response syndrome (SIRS), multiorgan dysfunction syndrome (MODS), and macrophage activation syndrome (MAS). Nevertheless, the therapeutic options for these are radically different. Chemotherapy and bone marrow transplant have been used for treatment of HLH/SHLH, whereas antibiotics and supportive treatment are used in severe sepsis/SIRS and MODS. MAS is treated with limited immune suppression. Outcomes are also different, SHLH has a mortality rate around 50%, whereas pediatric septic shock and MODS have a mortality of 10.3% and 18%, respectively, and severe sepsis in previously healthy children has a mortality rate of 2%. MAS has a mortality rate between 8% and 22%. Because SHLH and severe sepsis/SIRS/MODS/MAS share clinical and laboratory inflammatory phenotypes, we recommend extreme caution when considering applying HLH therapies to children with sepsis/SIRS/MODS/MAS. HLH therapies are clearly warranted for children with HLH; however, a quantitative functional estimate of cytotoxic lymphocyte function may be a more precise approach to define the overlap of these conditions, better identify these processes, and develop novel therapeutic protocols that may lead to improved treatments and outcomes.

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Year:  2009        PMID: 19325510     DOI: 10.1097/PCC.0b013e3181a1ae08

Source DB:  PubMed          Journal:  Pediatr Crit Care Med        ISSN: 1529-7535            Impact factor:   3.624


  83 in total

1.  Serum neopterin levels as a diagnostic marker of hemophagocytic lymphohistiocytosis syndrome.

Authors:  Maria F Ibarra; Marisa Klein-Gitelman; Elaine Morgan; Maria Proytcheva; Christine Sullivan; Gabrielle Morgan; Lauren M Pachman; Maurice R G O'Gorman
Journal:  Clin Vaccine Immunol       Date:  2011-01-26

2.  The CD68(+)/H-ferritin(+) cells colonize the lymph nodes of the patients with adult onset Still's disease and are associated with increased extracellular level of H-ferritin in the same tissue: correlation with disease severity and implication for pathogenesis.

Authors:  P Ruscitti; F Ciccia; P Cipriani; G Guggino; P Di Benedetto; A Rizzo; V Liakouli; O Berardicurti; F Carubbi; G Triolo; R Giacomelli
Journal:  Clin Exp Immunol       Date:  2015-12-08       Impact factor: 4.330

3.  Outcomes of adult critically ill patients with hemophagocytic lymphohistiocytosis in united states-analysis from an administrative database from 2007 to 2015.

Authors:  Gagan Kumar; Martin Hererra; Dhaval Patel; Rahul Nanchal; Achuta K Guddati
Journal:  Am J Blood Res       Date:  2020-12-15

4.  Cytokine Release Syndrome After Chimeric Antigen Receptor T Cell Therapy for Acute Lymphoblastic Leukemia.

Authors:  Julie C Fitzgerald; Scott L Weiss; Shannon L Maude; David M Barrett; Simon F Lacey; J Joseph Melenhorst; Pamela Shaw; Robert A Berg; Carl H June; David L Porter; Noelle V Frey; Stephan A Grupp; David T Teachey
Journal:  Crit Care Med       Date:  2017-02       Impact factor: 7.598

5.  Hemophagocytic lymphohistiocytosis: critical reappraisal of a potentially under-recognized condition.

Authors:  Somanath Padhi; Renu G' Boy Varghese; Anita Ramdas; Manjiri Dilip Phansalkar; RajLaxmi Sarangi
Journal:  Front Med       Date:  2013-10-14       Impact factor: 4.592

6.  Rescue of Cytokine Storm Due to HLH by Hemoadsorption in a CTLA4-Deficient Patient.

Authors:  Christine Greil; Fabian Roether; Paul La Rosée; Bodo Grimbacher; Daniel Duerschmied; Klaus Warnatz
Journal:  J Clin Immunol       Date:  2017-03-06       Impact factor: 8.317

7.  Understanding Disseminated Intravascular Coagulation and Hepatobiliary Dysfunction Multiple Organ Failure in Hyperferritinemic Critical Illness.

Authors:  Joseph A Carcillo; Bita Shakoory; Dennis Simon; Kate Kernan
Journal:  Pediatr Crit Care Med       Date:  2018-10       Impact factor: 3.624

8.  How We Manage Hyperferritinemic Sepsis-Related Multiple Organ Dysfunction Syndrome/Macrophage Activation Syndrome/Secondary Hemophagocytic Lymphohistiocytosis Histiocytosis.

Authors:  Joseph A Carcillo; Dennis W Simon; Bradley S Podd
Journal:  Pediatr Crit Care Med       Date:  2015-07       Impact factor: 3.624

9.  Chronic murine typhoid fever is a natural model of secondary hemophagocytic lymphohistiocytosis.

Authors:  Diane E Brown; Melissa W McCoy; M Carolina Pilonieta; Rebecca N Nix; Corrella S Detweiler
Journal:  PLoS One       Date:  2010-02-26       Impact factor: 3.240

10.  Immature cell populations and an erythropoiesis gene-expression signature in systemic juvenile idiopathic arthritis: implications for pathogenesis.

Authors:  Claas H Hinze; Ndate Fall; Sherry Thornton; Jun Q Mo; Bruce J Aronow; Gerlinde Layh-Schmitt; Thomas A Griffin; Susan D Thompson; Robert A Colbert; David N Glass; Michael G Barnes; Alexei A Grom
Journal:  Arthritis Res Ther       Date:  2010-06-24       Impact factor: 5.156

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