Mirja Puolakkainen

Mirja Puolakkainen

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Research Focus & Metrics

Academic Career Length

42Years (1985-Present)

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

Representative Publications

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1 January 2001 in Journal of NeuroVirology
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MKMarjaleena Koskiniemi
Marjaleena Koskiniemi
TRTimo Rantalaiho
Timo Rantalaiho
HPHeli Piiparinen
Heli Piiparinen
CBCarl-Henrik von Bonsdorff
Carl-Henrik von Bonsdorff
MFMarkus Färkkilä
Markus Färkkilä
SGStudy Group
Study Group
We studied 3231 patients with acute central nervous system (CNS) symptoms of suspected viral origin to elucidate the current etiologic spectrum. In 46% of the cases, a viral finding was observed....

6 June 2017 in Genome Research
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JHJames Hadfield
James Hadfield
SHSimon R. Harris
Simon R. Harris
HSHelena M.B. Seth-Smith
Helena M.B. Seth-Smith
SPSurendra Parmar
Surendra Parmar
PAPatiyan Andersson
Patiyan Andersson
NTNicholas R. Thomson
Nicholas R. Thomson
Chlamydia trachomatis is the world's most prevalent bacterial sexually transmitted infection and leading infectious cause of blindness, yet it is one of the least understood human pathogens, in part due to the difficulties of in vitro culturing and the lack of available tools for genetic manipulation. Genome sequencing has reinvigorated this field, shedding light on the contemporary history of this pathogen. Here, we analyze 563 full genomes, 455 of which are novel, to show that the history of the species comprises two phases, and conclude that the currently circulating lineages are the result of evolution in different genomic ecotypes. Temporal analysis indicates these lineages have recently expanded in the space of thousands of years, rather than the millions of years as previously thought, a finding that dramatically changes our understanding of this pathogen's history. Finally, at a time when almost every pathogen is becoming increasingly resistant to antimicrobials, we show that there is no evidence of circulating genomic resistance in C. trachomatis.

1 June 2000 in The Journal of Infectious Diseases
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RPRosanna W. Peeling
Rosanna W. Peeling
SWSan‐Pin Wang
San‐Pin Wang
JGJ. Thomas Grayston
J. Thomas Grayston
Francesco BlasiFrancesco Blasi
Francesco Blasi
JBJens Boman
Jens Boman
JSJulius Schachter
Julius Schachter
The lack of standardization in chlamydia serology has made interpretation of published data difficult. This study was initiated to determine the exte

2 May 1999 in Rheumatology
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THTimo Hannu
Timo Hannu
MPMirja Puolakkainen
Mirja Puolakkainen
MLM Leirisalo-Repo
M Leirisalo-Repo
OBJECTIVE: To determine the role of Chlamydia pneumoniae as a triggering infection in reactive arthritis (ReA). METHODS: Sixty patients with acute arthritis were screened for the evidence of triggering infections. In all patients, bacterial stool cultures, culture of Chlamydia trachomatis in urethra/cervix, and/or bacterial serology were studied. Chlamydia pneumoniae antibodies were measured by specific microimmunofluorescence test. RESULTS: Thirty-five of 60 patients fulfilled the diagnostic criteria for ReA. Thirty-one patients had microbial/serological evidence of preceding infection due to Salmonella, Yersinia, Campylobacter or Chlamydia trachomatis, or they had enteritis or urethritis prior to arthritis. Four additional patients had high antibody titre for C. pneumoniae. Three of these four patients had preceding lower respiratory symptoms, and were positive for HLA-B27. The clinical picture of C. pneumoniae-positive ReA patients was similar to that of ReA patients with other definite aetiology. CONCLUSION: Chlamydia pneumoniae is a triggering factor in approximately 10% of patients with acute ReA.

1 July 2000 in APMIS
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MGMesut Gencay
Mesut Gencay
MKMarjaleena Koskiniemi
Marjaleena Koskiniemi
PÄPirkko Ämmälä
Pirkko Ämmälä
VFVineta Fellman
Vineta Fellman
ANAle Närvänen
Ale Närvänen
MPMirja Puolakkainen
Mirja Puolakkainen

11 December 2020 in Pharmaceutics
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May Wenche JøraholmenMay Wenche Jøraholmen
May Wenche Jøraholmen
MJMona Johannessen
Mona Johannessen
KGKirsten Gravningen
Kirsten Gravningen
MPMirja Puolakkainen
Mirja Puolakkainen
GAGanesh Acharya
Ganesh Acharya
Natasa Skalko-BasnetNatasa Skalko-Basnet
Natasa Skalko-Basnet
Chlamydia trachomatis is the most common cause of bacterial sexually transmitted infections and causes serious reproductive tract complications among women. The limitations of existing oral antibiotics and treatment of antimicrobial resistance require alternative treatment options. We are proposing, for the first time, the natural polyphenol resveratrol (RES) in an advanced delivery system comprising liposomes incorporated in chitosan hydrogel, for the localized treatment of C. trachomatis infection. Both free RES and RES liposomes-in-hydrogel inhibited the propagation of C. trachomatis in a concentration-dependent manner, assessed by the commonly used in vitro model comprising McCoy cells. However, for lower concentrations, the anti-chlamydial effect of RES was enhanced when incorporated into a liposomes-in-hydrogel delivery system, with inhibition of 78% and 94% for 1.5 and 3 µg/mL RES, respectively for RES liposomes-in-hydrogel, compared to 43% and 72%, respectively, for free RES. Furthermore, RES liposomes-in-hydrogel exhibited strong anti-inflammatory activity in vitro, in a concentration-dependent inhibition of nitric oxide production in the LPS-induced macrophages (RAW 264.7). The combination of a natural substance exhibiting multi-targeted pharmacological properties, and a delivery system that provides enhanced activity as well as applicability for vaginal administration, could be a promising option for the localized treatment of C. trachomatis infection.