Leena Kainulainen
 


leena.kainulainen@utu.fi








Asiantuntijuusalueet
paediatrics; immunodeficiency; paediatric infectious diseases; respiratory infections; rhinovirus

Biografia



Docent
Leena Kainulainen graduated from medical school in 1995(University of Turku)
and defended her PhD theses on CVID in 2000. She received specialist licence in
paediatrics in 2005 and in pediatric infectious diseases 2013 and was appointed
as a docent in paediatrics in 2013 (University of Turku). She is currently
working as Head of the Division of Pediatric Care in Turku University Hospital
and as an immunology consultant at Department of Pediatrics and Medicine at
Turku University Hospital. She participates in neonatal screening for
severe immunodeficiencies.






Tutkimus



Docent
Kainulainen´s research is  focused on
primary immunodeficiency. Her current research interests comprise rhinovirus
infections in primary hypogammaglobulinemia patients. Clinical trial on the
treatment of rhinovirus infection with pegylated interferon alfa in CVID
patients is ongoing. Research project on innate immunity in autoimmune patients
is ongoing. In addition, she participates in research project aiming at  evaluating immunological status in pediatric
patients with neonatal cardiac surgery.






Opetus



Docent
Kainulainen has been working as a clinical lecturer in pediatrics 2004 and
2006. Currently she teaches regularly medical students and paediatric residents
as a part of her clinical duties.






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  • 22q11.2-deleetio-oireyhtymän hoito ja seuranta  (2025)  
    • Duodecim
     Wahrmann, Sakari; Strang-Karlsson, Sonja; Rajala, Katri; Koillinen, Hannele; Komulainen-Ebrahim, Jonna; Räsänen, Sami; Körkkö, Jarmo; Lindholm, Päivi; Ansamaa, Terhi; Keski-Filppula, Riikka; Lempainen, Johanna; Kainulainen, Leena; Wedenoja, Satu; Repo, Johanna; Kuismin, Outi
    (
    A2 Vertaisarvioitu katsausartikkeli tieteellisessä lehdessä)


  • Finnish nationwide controlled register study found increased inpatient infections in children with 22q11.2 deletion syndrome  (2024)  
    • Acta Paediatrica
     Wahrmann, Sakari; Kainulainen, Leena; Lempainen, Johanna; Kytö, Ville
    (
    A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä )


  • Genetic polymorphisms of TLR1, TLR2, TLR3 and TLR4 in patients with recurrent or severe infections  (2024)  
    • International Journal of Immunogenetics
     Teräsjärvi, Johanna; Kainulainen, Leena; Peltola, Ville; Mertsola, Jussi; Hakanen, Antti; He, Qiushui
    (
    A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä )


  • Primaariset immuunivajavuustilat  (2024)  Mikrobiologia, immunologia ja infektiosairaudet. Kirja 2, Immunologia  Kainulainen, Leena; Seppänen, Mikko
    (
    D2 Artikkeli ammatillisessa kokoomateoksessa)


  • Shorter birth length and decreased T-cell production and function predict severe infections in children with non-severe combined immunodeficiency cartilage-hair hypoplasia  (2024)  
    • Journal of Allergy and Clinical Immunology: Global
     Pello, Eetu; Kainulainen, Leena; Vakkilainen, Mikko; Klemetti, Paula; Taskinen, Mervi; Mäkitie, Outi; Vakkilainen, Svetlana
    (
    A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä )


  • Wiskott-Aldrich Syndrome: A study on 577 patients defining the genotype as a predictive biomarker for disease severity  (2024)  
    • Blood
     Vallée, Tanja C.; Glasmacher, Jannik S.; Buchner, Hannes; Arkwright, Peter D.; Behrends, Uta; Bondarenko, Anastasia; Browning, Michael J.; Buchbinder, David K.; Cattoni, Alessandro; Chernyshova, Liudmyla; Ciznar, Peter; Cole, Theresa; Czogala, Wojciech; Dueckers, Gregor; Edgar, John David M.; Erbey, Fatih; Fasth, Anders; Ferrua, Francesca; Formankova, Renata; Gambineri, Eleonora; Gennery, Andrew R.; Goldman, Frederick D.; Gonzalez-Granado, Luis Ignacio; Heilmann, Carsten; Heiskanen-Kosma, Tarja; Juntti, Hanna; Kainulainen, Leena; Kanegane, Hirokazu; Karaca, Neslihan E.; Sebnem Kilic, Sara; Klein, Christoph; Koltan, Sylwia; Kondratenko, Irina; Meyts, Isabelle; Nasrullayeva, Gulnara M.; Notarangelo, Lucia Dora; Pasic, Srdjan; Pellier, Isabelle; Pignata, Claudio; Misbah, Siraj Ahmed; Schulz, Ansgar S.; Segundo, Gesmar R. S.; Shcherbina, Anna; Slatter, Mary A.; Sokolic, Robert; Soler-Palacin, Pere; Stepensky, Polina; van Montfrans, Joris M.; Ryhänen, Samppa; Wolska-Kuśnierz, Beata; Ziegler, John B.; Zhao, Xiaodong; Aiuti, Alessandro; Ochs, Hans D.; Albert, Michael H.
    (
    A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä )


  • Childhood manifestations of 22q11.2 deletion syndrome: A Finnish nationwide register-based cohort study  (2023)  
    • Acta Paediatrica
     Wahrmann Sakari, Kainulainen Leena, Kytö Ville, Lempainen Johanna
    (
    A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä )


  • Monogenic early-onset lymphoproliferation and autoimmunity: Natural history of STAT3 gain-of-function syndrome  (2023)  
    • Journal of Allergy and Clinical Immunology
     Leiding Jennifer W, Vogel Tiphanie P, Santarlas Valentine GJ, Mhaskar Rahul, Smith Madison R, Carisey Alexandre, Vargas-Hernández Alexander, Silva-Carmona Manuel, Heeg Maximilian, Rensing-Ehl Anne, Neven Bénédicte, Hadjadj Jérôme, Hambleton Sophie, Ronan Leahy Timothy, Meesilpavikai Kornvalee, Cunningham-Rundles Charlotte, Dutmer Cullen M, Sharapova Svetlana O, Taskinen Mervi, Chua Ignatius, Hague Rosie, Klemann Christian, Kostyuchenko Larysa, Morio Tomohiro, Thatayatikom Akaluck, Ozen Ahmet, Scherbina Anna, Bauer Cindy S, Flanagan Sarah E, Gambineri Eleonora, Giovannini-Chami Lisa, Heimall Jennifer, Sullivan Kathleen E, Allenspach Eric, Romberg Neil, Deane Sean G, Prince Benjamin T, Rose Melissa J, Bohnsack John, Mousallem Talal, Jesudas Rohit, Santos Vilela Maria Marluce Dos, O'Sullivan Michael, Pachlopnik Schmid Jana, Průhová Štěpánka, Klocperk Adam, Rees Matthew, Su Helen, Bahna Sami, Baris Safa, Bartnikas Lisa M, Chang Berger Amy, Briggs Tracy A, Brothers Shannon, Bundy Vanessa, Chan Alice Y, Chandrakasan Shanmuganathan, Christiansen Mette, Cole Theresa, Cook Matthew C, Desai Mukesh M, Fischer Ute, Fulcher David A, Gallo Silvanna, Gauthier Amelie, Gennery Andrew R, Gonçalo Marques José, Gottrand Frédéric, Grimbacher Bodo, Grunebaum Eyal, Haapaniemi Emma, Hämäläinen Sari, Heiskanen Kaarina, Heiskanen-Kosma Tarja, Hoffman Hal M, Gonzalez-Granado Luis Ignacio, Guerrerio Anthony L, Kainulainen Leena, Kumar Ashish, Lawrence Monica G, Levin Carina, Martelius Timi, Neth Olaf, Olbrich Peter, Palma Alejandro, Patel Niraj C, Pozos Tamara, Preece Kahn, Lugo Reyes Saúl Oswaldo, Russell Mark A, Schejter Yael, Seroogy Christine, Sinclair Jan, Skevofilax Effie, Suan Daniel, Suegeorgz Daniel, Szabolcs Paul, Velasco Helena, Warnatz Klaus, Walkovich Kelly, Worth Austen; STAT3 GOF Working Group members, Seppänen Mikko RJ, Torgerson Troy R, Sogkas Georgios, Ehl Stephan, Tangye Stuart G, Cooper Megan A, Milner Joshua D, Forbes Satter Lisa R
    (
    A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä )


  • Overlap between EEC and AEC syndrome and immunodeficiency in a preterm infant with a TP63 variant  (2023)  
    • European Journal of Medical Genetics
     Helenius Kjell, Ojala Liisa, Kainulainen Leena, Peltonen Sirkku, Hietala Marja, Pohjola Pia, Parikka Vilhelmiina
    (
    A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä )


  • Tavallisimmat primaarit immuunipuutokset  (2023)  Lastentaudit Helminen Merja, Kainulainen Leena
    (
    D2 Artikkeli ammatillisessa kokoomateoksessa)



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