Peter Engelmann

Dr. Peter Engelmann

Department of Immunology and Biotechnology, Medical School, University of Pécs, Pécs, Hungary
orcid

Research Focus & Metrics

Academic Career Length

25Years (2002-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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20 March 2012 in Environmental Science & Technology
Verified
Journal Article
Closed access
YHYuya Hayashi
Yuya Hayashi
PEPeter Engelmann
Peter Engelmann
RFRasmus Foldbjerg
Rasmus Foldbjerg
MSMariann Szabó
Mariann Szabó
ISIldikó Somogyi
Ildikó Somogyi
LHLars-Henrik Heckmann
Lars-Henrik Heckmann

18 November 2013 in Environmental Science & Technology
Verified
Journal Article
Closed access
YHYuya Hayashi
Yuya Hayashi
TMTeodora Miclaus
Teodora Miclaus
CSCarsten Scavenius
Carsten Scavenius
KKKatarzyna Kwiatkowska
Katarzyna Kwiatkowska
ASAndrzej Sobota
Andrzej Sobota
DSDuncan Sutherland
Duncan Sutherland

1 June 2004 in Cell and tissue research
Verified
Journal Article
Closed access
PDF file
PEPeter Engelmann
Peter Engelmann
ECE. L. Cooper
E. L. Cooper
Molnár LászlóMolnár László
Molnár László
LPL. Pálinkás
L. Pálinkás
PNP. Németh
P. Németh

6 December 2006 in Journal of Leukocyte Biology
Verified
Journal Article
Open access
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JKJanos Kis
Janos Kis
PEPeter Engelmann
Peter Engelmann
KFKlara Farkas
Klara Farkas
GRGeoffrey Richman
Geoffrey Richman
SEShawn Eck
Shawn Eck
TOTihamer Orban
Tihamer Orban
Invariant NKT (iNKT) cells are considered to be important in some autoimmune diseases including Type 1 diabetes mellitus (T1DM). So far, the published data are contradictory in regard to the role of iNKT cells in T1DM. We aimed to study iNKT cell frequency and the function of different iNKT cell subgroups in T1DM. We compared the results of four subject groups: healthy (H), long-term T2DM (ltT2DM; more than 1 year), newly diagnosed T1DM (ndT1DM; less than 3 months), and ltT1DM (more than 1 year) individuals. We measured the iNKT cell frequencies by costaining for the invariant TCR α-chain with 6B11-FITC and Vα24-PE. After sorting the Vα24+6B11+ cells, the generated iNKT clones were characterized. We tested CD4, CD8, and CD161 expression and IL-4 and IFN-γ production on TCR stimulation. The CD4+ population among the iNKT cells was decreased significantly in ltT1DM versus ndT1DM, ltT2DM, or H individuals. The T1DM iNKT cell cytokine profile markedly shifted to the Th1 direction. There was no difference in the frequency of iNKT cells in PBMC among the different patient groups. The decrease in the CD4+ population among the iNKT cells and their Th1 shift indicates dysfunction of these potentially important regulatory cells in T1DM.

4 December 2007 in Journal of Immunology Research
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Journal Article
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KKKrisztian Kvell
Krisztian Kvell
ECEl. Cooper
El. Cooper
PEPeter Engelmann
Peter Engelmann
JBJ. Bovari
J. Bovari
PNP. Nemeth
P. Nemeth
Adaptive immunity has often been considered the penultimate of immune capacities. That system is now being deconstructed to encompass less stringent rules that govern its initiation, actual effector activity, and ambivalent results. Expanding the repertoire of innate immunity found in all invertebrates has greatly facilitated the relaxation of convictions concerning what actually constitutes innate and adaptive immunity. Two animal models, incidentally not on the line of chordate evolution (C. elegansandDrosophila), have contributed enormously to defining homology. The characteristics of specificity and memory and whether the antigen is pathogenic or nonpathogenic reveal considerable information on homology, thus deconstructing the more fundamentalist view. Senescence, cancer, and immunosuppression often associated with mammals that possess both innate and adaptive immunity also exist in invertebrates that only possess innate immunity. Strict definitions become blurred casting skepticism on the utility of creating rigid definitions of what innate and adaptive immunity are without considering overlaps.