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2. Reconstitution of the uterine immune milieu after transplantation

Author

Strunz, Benedikt, primary, Ivarsson, Martin A., additional, Sun, Dan, additional, Ziegenhain, Christoph, additional, Crona-Guterstam, Ylva, additional, Solders, Martin, additional, Björklund, Andreas, additional, Marquardt, Nicole, additional, Kaipe, Helen, additional, Flöter-Rådestad, Angelique, additional, Gidlöf, Sebastian, additional, Brännström, Mats, additional, and Björkström, Niklas K., additional

Published
2024
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4. Tissue-specific nonheritable influences drive endometrial immune system variation.

Author

Bister, Jonna, Filipovic, Iva, Sun, Dan, Crona-Guterstam, Ylva, Cornillet, Martin, Ponzetta, Andrea, Michaëlsson, Jakob, Gidlöf, Sebastian, Ivarsson, Martin A., Strunz, Benedikt, and Björkström, Niklas K.

Subjects
IMMUNE system, MONOZYGOTIC twins, CYTOMEGALOVIRUS diseases, BLOOD cells, TWIN studies
Abstract

Although human twin studies have revealed the combined contribution of heritable and environmental factors in shaping immune system variability in blood, the contribution of these factors to immune system variability in tissues remains unexplored. The human uterus undergoes constant regeneration and is exposed to distinct environmental factors. To assess uterine immune system variation, we performed a system-level analysis of endometrial and peripheral blood immune cells in monozygotic twins. Although most immune cell phenotypes in peripheral blood showed high genetic heritability, more variation was found in endometrial immune cells, indicating a stronger influence by environmental factors. Cytomegalovirus infection was identified to influence peripheral blood immune cell variability but had limited effect on endometrial immune cells. Instead, hormonal contraception shaped the local endometrial milieu and immune cell composition with minor influence on the systemic immune system. These results highlight that the magnitude of human immune system variation and factors influencing it can be tissue specific. Editor's summary: Baseline differences in the immune system between individuals are driven by both heritable and nonheritable, environmental factors. By analyzing endometrial and peripheral blood immune cells collected from monozygotic twins, Bister et al. measured the tissue-specific contributions of nonheritable effects on immune system variation. Although peripheral blood immune cells were largely shaped by genetics, environmental factors including hormonal contraception contributed more strongly to the variation in endometrial immune cells and soluble proteome. Together, these findings demonstrate that the human immune system can be highly variable and driven by nonheritable factors in a tissue-specific manner. —Claire Olingy [ABSTRACT FROM AUTHOR]

Published
2024
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6. Single-cell reconstruction of the early maternal–fetal interface in humans

Author

Vento-Tormo, Roser, Efremova, Mirjana, Botting, Rachel A., Turco, Margherita Y., Vento-Tormo, Miquel, Meyer, Kerstin B., Park, Jong-Eun, Stephenson, Emily, Polański, Krzysztof, Goncalves, Angela, Gardner, Lucy, Holmqvist, Staffan, Henriksson, Johan, Zou, Angela, Sharkey, Andrew M., Millar, Ben, Innes, Barbara, Wood, Laura, Wilbrey-Clark, Anna, Payne, Rebecca P., Ivarsson, Martin A., Lisgo, Steve, Filby, Andrew, Rowitch, David H., Bulmer, Judith N., Wright, Gavin J., Stubbington, Michael J. T., Haniffa, Muzlifah, Moffett, Ashley, and Teichmann, Sarah A.

Published
2018
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10. Immune cell profiling of vaginal blood from patients with early pregnancy bleeding.

Author

Guterstam, Ylva Crona, Acharya, Ganesh, Schott, Katharina, Björkström, Niklas K., Gidlöf, Sebastian, and Ivarsson, Martin A.

Subjects
PREGNANCY outcomes, MISCARRIAGE, KILLER cells, BLOOD cells, UTERINE hemorrhage
Abstract

Problem: Vaginal bleeding during early pregnancy is estimated to occur in 20% of all pregnancies and it is often difficult to predict who will ultimately miscarry. The role of immune cells in early pregnancy loss is poorly understood. Method of Study: In this prospective cohort study, 28 pregnant women presenting with first‐trimester vaginal bleeding donated vaginal blood, peripheral venous blood, and saliva during their initial emergency room visit, and at a follow‐up. The composition, frequency, and phenotype of immune cells in the vaginal blood were determined using flow cytometry. The proteome of serum and saliva was analyzed with OLINK proximity extension assay and correlated to vaginal immune cell phenotype and outcome of pregnancy. The course and outcome of pregnancies were followed and recorded. Results: Vaginal blood contained all main immune cell lineages including B cells, NK cells, T cells, and monocytes/macrophages. Notably, vaginal blood immune cells expressed tissue residency markers including CD49a. Women who subsequently miscarried had a higher frequency of vaginal blood CD49a+ NK cells compared to those who did not miscarry, and this correlated with serum levels of granzyme A and H, as well as CSF1, CAIX, and TWEAK. Women in the miscarriage group also had a higher frequency of peripheral blood T cells expressing CD49a. Conclusions: Our study provides novel insight into human reproductive immunology in relation to miscarriage. Tissue‐resident NK cells in vaginal blood alone or in combination with serological biomarkers hold potential as prognostic factors in the prediction of pregnancy outcome in women with early pregnancy bleedings. [ABSTRACT FROM AUTHOR]

Published
2023
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11. Improved Control of Automotive Software Suppliers

Author

Ivarsson, Martin, Pettersson, Fredrik, Öhman, Peter, Hutchison, David, editor, Kanade, Takeo, editor, Kittler, Josef, editor, Kleinberg, Jon M., editor, Mattern, Friedemann, editor, Mitchell, John C., editor, Naor, Moni, editor, Nierstrasz, Oscar, editor, Pandu Rangan, C., editor, Steffen, Bernhard, editor, Sudan, Madhu, editor, Terzopoulos, Demetri, editor, Tygar, Dough, editor, Vardi, Moshe Y., editor, Weikum, Gerhard, editor, Bomarius, Frank, editor, and Komi-Sirviö, Seija, editor

Published
2005
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15. Differentiation and functional regulation of human fetal NK cells

Author

Ivarsson, Martin A., Loh, Liyen, Marquardt, Nicole, Kekalainen, Eliisa, Berglin, Lena, Bjorkstrom, Niklas K., Westgren, Magnus, Nixon, Douglas F., and Michaelsson, Jakob

Subjects
Fetal tissues -- Physiological aspects -- Research, Killer cells -- Physiological aspects -- Research, Cell differentiation -- Research, Health care industry
Abstract

The human fetal immune system is naturally exposed to maternal allogeneic cells, maternal antibodies, and pathogens. As such, it is faced with a considerable challenge with respect to the balance [...]

Published
2013

19. Continuous human uterine NK cell differentiation in response to endometrial regeneration and pregnancy

Author

Strunz, Benedikt, primary, Bister, Jonna, additional, Jönsson, Hanna, additional, Filipovic, Iva, additional, Crona-Guterstam, Ylva, additional, Kvedaraite, Egle, additional, Sleiers, Natalie, additional, Dumitrescu, Bogdan, additional, Brännström, Mats, additional, Lentini, Antonio, additional, Reinius, Björn, additional, Cornillet, Martin, additional, Willinger, Tim, additional, Gidlöf, Sebastian, additional, Hamilton, Russell S., additional, Ivarsson, Martin A., additional, and Björkström, Niklas K., additional

Published
2021
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20. The Identity of Human Tissue-Emigrant CD8+ T Cells

Author

Buggert, Marcus, primary, Vella, Laura A., additional, Nguyen, Son, additional, Wu, Vincent H., additional, Chen, Zeyu, additional, Sekine, Takuya, additional, Perez-Potti, André, additional, Maldini, Colby R., additional, Manne, Sasikanth, additional, Darko, Samuel, additional, Ransier, Amy, additional, Kuri-Cervantes, Leticia, additional, Japp, Alberto Sada, additional, Brody, Irene Bukh, additional, Ivarsson, Martin A., additional, Gorin, Jean-Baptiste, additional, Rivera-Ballesteros, Olga, additional, Hertwig, Laura, additional, Antel, Jack P., additional, Johnson, Matthew E., additional, Okoye, Afam, additional, Picker, Louis, additional, Vahedi, Golnaz, additional, Sparrelid, Ernesto, additional, Llewellyn-Lacey, Sian, additional, Gostick, Emma, additional, Sandberg, Johan K., additional, Björkström, Niklas, additional, Bar-Or, Amit, additional, Dori, Yoav, additional, Naji, Ali, additional, Canaday, David H., additional, Laufer, Terri M., additional, Wells, Andrew D., additional, Price, David A., additional, Frank, Ian, additional, Douek, Daniel C., additional, Wherry, E. John, additional, Itkin, Maxim G., additional, and Betts, Michael R., additional

Published
2020
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21. The cytokine profile of menstrual blood

Author

Crona Guterstam, Ylva, primary, Strunz, Benedikt, additional, Ivarsson, Martin A., additional, Zimmer, Christine, additional, Melin, Anna‐Sofia, additional, Jonasson, Aino F., additional, Björkström, Niklas K., additional, and Gidlöf, Sebastian Brusell, additional

Published
2020
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22. The identity of human tissue-emigrant CD8+T cells

Author

Buggert, Marcus, primary, Vella, Laura A., additional, Nguyen, Son, additional, Wu, Vincent, additional, Sekine, Takuya, additional, Perez-Potti, André, additional, Maldini, Colby R., additional, Manne, Sasikanth, additional, Darko, Samuel, additional, Ransier, Amy, additional, Kuri-Cervantes, Leticia, additional, Japp, Alberto Sada, additional, Brody, Irene Bukh, additional, Ivarsson, Martin A., additional, Hertwig, Laura, additional, Antel, Jack P., additional, Johnson, Matthew E., additional, Okoye, Afam, additional, Picker, Louis, additional, Vahedi, Golnaz, additional, Sparrelid, Ernesto, additional, Llewellyn-Lacey, Sian, additional, Gostick, Emma, additional, Björkström, Niklas, additional, Bar-Or, Amit, additional, Dori, Yoav, additional, Naji, Ali, additional, Canaday, David H., additional, Laufer, Terri M., additional, Wells, Andrew D., additional, Price, David A., additional, Frank, Ian, additional, Douek, Daniel C., additional, Wherry, E. John, additional, Itkin, Maxim G., additional, and Betts, Michael R., additional

Published
2020
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25. Activating KIR2DS4 Is Expressed by Uterine NK Cells and Contributes to Successful Pregnancy

Author

Kennedy, Philippa R., Chazara, Olympe, Gardner, Lucy, Ivarsson, Martin A., Farrell, Lydia E., Xiong, Shiqiu, Hiby, Susan E., Colucci, Francesco, Sharkey, Andrew M., Moffett, Ashley, Colucci, Francesco [0000-0001-5193-6376], Sharkey, Andrew [0000-0002-5072-7748], Moffett, Ashley [0000-0002-8388-9073], and Apollo - University of Cambridge Repository

Subjects
Immunology, Granulocyte-Macrophage Colony-Stimulating Factor, Cell Line, Trophoblasts, Killer Cells, Natural, Gene Expression Regulation, Receptors, KIR, Pregnancy, embryonic structures, Decidua, Humans, Clinical and Human Immunology, Female
Abstract

Tissue-specific NK cells are abundant in the pregnant uterus and interact with invading placental trophoblast cells that transform the maternal arteries to increase the fetoplacental blood supply. Genetic case-control studies have implicated killer cell Ig-like receptor (KIR) genes and their $\textit{HLA}$ ligands in pregnancy disorders characterized by failure of trophoblast arterial transformation. Activating $\textit{KIR2DS1}$ or $\textit{KIR2DS5}$ (when located in the centromeric region as in Africans) lower the risk of disorders when there is a fetal $\textit{HLA-C}$ allele carrying a C2 epitope. In this study, we investigated another activating $\textit{KIR, KIR2DS4}$, and provide genetic evidence for a similar effect when carried with $\textit{KIR2DS1. KIR2DS4}$ is expressed by ∼45% of uterine NK (uNK) cells. Similarly to KIR2DS1, triggering of KIR2DS4 on uNK cells led to secretion of GM-CSF and other chemokines, known to promote placental trophoblast invasion. Additionally, XCL1 and CCL1, identified in a screen of 120 different cytokines, were consistently secreted upon activation of KIR2DS4 on uNK cells. Inhibitory $\textit{KIR2DL5A}$, carried in linkage disequilibrium with $\textit{KIR2DS1}$, is expressed by peripheral blood NK cells but not by uNK cells, highlighting the unique phenotype of uNK cells compared with peripheral blood NK cells. That KIR2DS4, KIR2DS1, and some alleles of KIR2DS5 contribute to successful pregnancy suggests that activation of uNK cells by KIR binding to HLA-C is a generic mechanism promoting trophoblast invasion into the decidua.

Published
2016

26. Verifiering av P-LDL-kolesterol på Beckman Coulter AU680

Author

Oliveira Ivarsson, Martin

Subjects
Beckman Coulter AU680, LDL-kolesterol, method verification, Klinisk laboratoriemedicin, LDL-Cholesterol, Clinical Laboratory Medicine, metodverifiering, lipids (amino acids, peptides, and proteins)
Abstract

Kolesterol transporteras i blodet med hjälp av lipoproteinpartiklar. Höga nivåer av low-density lipoprotein (LDL)-kolesterol i blodet är en riskfaktor för kardiovaskulär sjukdom. Koncentrationen av LDL-kolesterol kan beräknas med hjälp av Friedewalds formel men det finns även metoder där LDL-kolesterol kan analyseras direkt. Syftet med arbetet var att verifiera metoden direkt LDL-kolesterol på analysinstrumentet Beckman Coulter AU680. Metodens inomserie- och totalimprecision analyserades. Två korrelationsstudier utfördes mellan direkt LDL-kolesterol och beräknat LDL-kolesterol, en med 43 patientprover med triglycerider < 4,5 mmol/L och en med 11 patientprover med triglycerider > 4,5 mmol/L. Friedewalds formel ska egentligen inte användas vid triglycerider > 4,5 mmol/L, men i detta fall användes formeln ändå för att utvärdera eventuella skillnader mellan metodernas resultat vid höga triglyceridkoncentrationer. Vid analys av metodens inomserieimprecision blev variationskoefficienten (CV) omkring 0,5 % vid analys av både den låga kontrollen (A1) och den höga kontrollen (A2). CV för totalimprecisionen blev 1,21 % vid analys av A1 och 1,11 % vid analys av A2. Korrelationsstudierna visade ett linjärt samband mellan metoderna men den direkta metoden gav något högre resultat vid lägre koncentrationer och något lägre resultat vid högre koncentrationer jämfört med beräknat LDL-kolesterol. Vid triglycerider > 4,5 mmol/L gav den direkta metoden betydligt högre resultat än beräknat LDL-kolesterol. Slutsatsen blev att metoden hade god precision. Överensstämmelsen mellan metodernas resultat var relativt bra för proverna med triglycerider < 4,5 mmol/L. Vid triglycerider > 4,5 mmol/L var differensen mellan metoderna stor, troligtvis på grund av falskt för låga resultat från beräknat LDL-kolesterol. Cholesterol is transported in the blood by lipoproteins. High levels of low-density lipoprotein (LDL)-cholesterol in the blood is a risk factor for cardiovascular disease. The concentration of LDL-cholesterol can be calculated using the Friedewald formula but there are also methods that measure LDL-cholesterol directly. The aim of this study was to verify the method P-LDL-cholesterol on a Beckman Coulter AU680 analyzer. Within-run imprecision and total imprecision were analyzed. The correlation between direct LDL-cholesterol and calculated LDL-cholesterol was examined using 43 patient samples with triglyceride levels < 4,5 mmol/L and 11 patient samples with triglyceride levels > 4,5 mmol/L. The Friedewald formula is not supposed to be used on triglyceride levels > 4,5 mmol/L, but in this case the formula was used anyway to evaluate differences between the methods at high triglyceride concentrations. The coefficient of variation (CV) for the within-run imprecision was about 0,5 %, both for the low control (A1) and the high control (A2). Total imprecision had a CV of 1,21 % for A1 and 1,11 % for A2. There was a linear relationship between the methods, but the direct method gave slightly higher results at low concentrations and slightly lower results at high concentrations compared to calculated LDL-cholesterol. At triglyceride levels > 4,5 mmol/L the results from the direct method was considerably higher than calculated LDL-cholesterol. The conclusion is that the precision of the method was good. The correlation between the results from direct LDL-cholesterol and calculated LDL-cholesterol was relatively high for samples with triglyceride levels < 4,5 mmol/L. At triglyceride levels > 4,5 mmol/L there was a big difference between the methods, probably because of falsely low results from calculated LDL-cholesterol.

Published
2019

28. Correction: High-Resolution Genetic and Phenotypic Analysis of KIR2DL1 Alleles and Their Association with Pre-Eclampsia

Author

Huhn, Oisín, primary, Chazara, Olympe, additional, Ivarsson, Martin A., additional, Retière, Christelle, additional, Venkatesan, Timothy C., additional, Norman, Paul J., additional, Hilton, Hugo G., additional, Jayaraman, Jyothi, additional, Traherne, James A., additional, Trowsdale, John, additional, Ito, Mitsutero, additional, Kling, Christiane, additional, Parham, Peter, additional, Ghadially, Hormas, additional, Moffett, Ashley, additional, Sharkey, Andrew M., additional, and Colucci, Francesco, additional

Published
2019
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29. High-Resolution Genetic and Phenotypic Analysis of KIR2DL1 Alleles and Their Association with Pre-Eclampsia

Author

Huhn, Oisín, primary, Chazara, Olympe, additional, Ivarsson, Martin A., additional, Retière, Christelle, additional, Venkatesan, Timothy C., additional, Norman, Paul J., additional, Hilton, Hugo G., additional, Jayaraman, Jyothi, additional, Traherne, James A., additional, Trowsdale, John, additional, Ito, Mitsutero, additional, Kling, Christiane, additional, Parham, Peter, additional, Ghadially, Hormas, additional, Moffett, Ashley, additional, Sharkey, Andrew M., additional, and Colucci, Francesco, additional

Published
2018
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31. The cytokine profile of menstrual blood.

Author

Crona Guterstam, Ylva, Strunz, Benedikt, Ivarsson, Martin A., Zimmer, Christine, Melin, Anna‐Sofia, Jonasson, Aino F., Björkström, Niklas K., Gidlöf, Sebastian Brusell, and Melin, Anna-Sofia

Subjects
BLOOD plasma, LUTEAL phase, MENSTRUAL cycle, BLOOD, EMBRYO implantation, CYTOKINES, RESEARCH, BIOPSY, RESEARCH methodology, MENSTRUATION, EVALUATION research, MEDICAL cooperation, COMPARATIVE studies, RESEARCH funding, ENDOMETRIUM
Abstract

Introduction: The menstrual cycle is regulated by a complex interplay between endometrial epithelial cells, endothelial cells, immune cells, and sex hormones. To communicate, cells secrete cytokines that have multiple and diverse effects on recipient cells. Knowledge of how these cells interact in the uterus is insufficient. Menstrual blood is easily accessible and provides a source to study menstrual cycle physiology. This study aimed to determine the cytokine profile in menstrual blood plasma and investigate the differences in cytokine profiles between menstrual and peripheral blood plasma. Several previous studies indicate an improved chance of embryo implantation after endometrial scratching. Consequently, our secondary aim was to compare the menstrual blood cytokine profile before and after luteal phase endometrial scratching.Material and Methods: Nineteen healthy donors collected menstrual blood for the first 24 hours of menstruation in two sequential cycles. Matched peripheral blood was taken at the same time. An endometrial biopsy was performed at cycle day 7-9 post ovulation in between the two collection times. A Luminex multiplex assay was performed in one batch analyzing a predetermined group of cytokines in plasma.Results: Peripheral blood plasma and menstrual blood plasma showed substantial significant differences in cytokine profile. In menstrual blood plasma, C5/C5a, interleukin-6 (IL-6), IL-1β, and CXCL8 were detected in high concentrations, whereas IL-2, IL-12p70, XCL1/Lymphotactin, and interferon-γ were low. The most pronounced median differences between menstrual and peripheral blood plasma were found for IL-6, IL-1β, and CXCL8. The cytokine profiles of menstrual blood plasma were similar between the individual donors and did not differ over two subsequent cycles. None of the cytokines analyzed in menstrual blood plasma differed significantly before or after luteal phase endometrial scratching (P < .01).Conclusions: Our results demonstrate that the menstrual blood cytokine profile is distinctly different from peripheral blood plasma and that the inter-individual difference in menstrual blood cytokine profile in healthy donors is limited and stable over time. The small injury caused by an endometrial biopsy does not change the cytokine profile in the subsequent menstrual cycle. Our study provides new insights into menstrual cycle physiology. [ABSTRACT FROM AUTHOR]

Published
2021
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33. Maintenance of Christmas trees and Christmas tree cultivations in Sweden

Author

Ivarsson, Martin

Subjects
Skogsvetenskap, Christmas tree cultivators, Forest Science, Chrismas tree maintenance
Abstract

Unlike Sweden, Denmark is a major industry when it comes to christmas tree cultivation. More than ten million christmas trees are processed in Denmark annually. The primary purpose of this report is to investigate the technology, treatment and maintenance of christmas trees in Sweden and Denmark, and to find differences in the management between Swedish and Danish christmas tree cultivators. Since an opinion poll has been made, the investigation method mainly used for this report is quantitative. But a qualitative investigation method has also been used to some extent as a few unstructured interviews has occurred while visiting a couple of the cultivators. 63 % of the christmas tree cultivators consider themselves knowledgeable about christmas tree cultivation and 68 % wants to learn more. There is both similarities and differences along those cultivators that has been visited. Obvious similarities has mostly been found when visiting farms engaged in developing christmas trees to a bigger extent. Denmark conducts their maintenance methods with the aim to produce a large amount of high quality Christmas trees. This tendency does also occur in Sweden at, for example, Gunnars Granar located in Degeberga. Gunnar manages his cultivation almost identically to Denmark's management methods. However, the big christmas tree cultivators are still mainly located in Denmark.

Published
2016

34. Human lung natural killer cells are predominantly comprised of highly differentiated hypofunctional CD69 − CD56 dim cells

Author

Marquardt, Nicole, primary, Kekäläinen, Eliisa, additional, Chen, Puran, additional, Kvedaraite, Egle, additional, Wilson, Jennifer N., additional, Ivarsson, Martin A., additional, Mjösberg, Jenny, additional, Berglin, Lena, additional, Säfholm, Jesper, additional, Manson, Martijn L., additional, Adner, Mikael, additional, Al-Ameri, Mamdoh, additional, Bergman, Per, additional, Orre, Ann-Charlotte, additional, Svensson, Mattias, additional, Dahlén, Barbro, additional, Dahlén, Sven-Erik, additional, Ljunggren, Hans-Gustaf, additional, and Michaëlsson, Jakob, additional

Published
2017
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36. Fetal CD103+ IL-17–Producing Group 3 Innate Lymphoid Cells Represent the Dominant Lymphocyte Subset in Human Amniotic Fluid

Author

Marquardt, Nicole, primary, Ivarsson, Martin A., additional, Sundström, Erik, additional, Åkesson, Elisabet, additional, Martini, Elisa, additional, Eidsmo, Liv, additional, Mjösberg, Jenny, additional, Friberg, Danielle, additional, Kublickas, Marius, additional, Ek, Sverker, additional, Tegerstedt, Gunilla, additional, Seiger, Åke, additional, Westgren, Magnus, additional, and Michaëlsson, Jakob, additional

Published
2016
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37. The Human NK Cell Response to Yellow Fever Virus 17D Is Primarily Governed by NK Cell Differentiation Independently of NK Cell Education

Author

Marquardt, Nicole, primary, Ivarsson, Martin A., additional, Blom, Kim, additional, Gonzalez, Veronica D., additional, Braun, Monika, additional, Falconer, Karolin, additional, Gustafsson, Rasmus, additional, Fogdell-Hahn, Anna, additional, Sandberg, Johan K., additional, and Michaëlsson, Jakob, additional

Published
2015
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38. Tissue-Specific Education of Decidual NK Cells

Author

Sharkey, Andrew M., primary, Xiong, Shiqiu, additional, Kennedy, Philippa R., additional, Gardner, Lucy, additional, Farrell, Lydia E., additional, Chazara, Olympe, additional, Ivarsson, Martin A., additional, Hiby, Susan E., additional, Colucci, Francesco, additional, and Moffett, Ashley, additional

Published
2015
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39. Cutting Edge: Identification and Characterization of Human Intrahepatic CD49a+ NK Cells

Author

Marquardt, Nicole, primary, Béziat, Vivien, additional, Nyström, Sanna, additional, Hengst, Julia, additional, Ivarsson, Martin A., additional, Kekäläinen, Eliisa, additional, Johansson, Helene, additional, Mjösberg, Jenny, additional, Westgren, Magnus, additional, Lankisch, Tim O., additional, Wedemeyer, Heiner, additional, Ellis, Ewa C., additional, Ljunggren, Hans-Gustaf, additional, Michaëlsson, Jakob, additional, and Björkström, Niklas K., additional

Published
2015
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40. T-bet and Eomes Are Differentially Linked to the Exhausted Phenotype of CD8+ T Cells in HIV Infection

Author

Buggert, Marcus, primary, Tauriainen, Johanna, additional, Yamamoto, Takuya, additional, Frederiksen, Juliet, additional, Ivarsson, Martin A., additional, Michaëlsson, Jakob, additional, Lund, Ole, additional, Hejdeman, Bo, additional, Jansson, Marianne, additional, Sönnerborg, Anders, additional, Koup, Richard A., additional, Betts, Michael R., additional, and Karlsson, Annika C., additional

Published
2014
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41. Tracing dynamic expansion of human NK ‐cell subsets by high‐resolution analysis of KIR repertoires and cellular differentiation

Author

Béziat, Vivien, primary, Traherne, James, additional, Malmberg, Jenny‐Ann, additional, Ivarsson, Martin A., additional, Björkström, Niklas K., additional, Retière, Christelle, additional, Ljunggren, Hans‐Gustaf, additional, Michaëlsson, Jakob, additional, Trowsdale, John, additional, and Malmberg, Karl‐Johan, additional

Published
2014
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