Sir Frank Macfarlane Burnet 1899–1985 - p1009

doi:10.1038/ni1007-1009

Full Text - Sir Frank Macfarlane Burnet 1899–1985 | PDF (126 KB) - Sir Frank Macfarlane Burnet 1899–1985

Edward A. Boyse 1923–2007 - pp1011 - 1012

Judith Bard, Gary K Beauchamp & Ellen H Goldberg

doi:10.1038/ni1007-1011

Full Text - Edward A. Boyse 1923–2007 | PDF (104 KB) - Edward A. Boyse 1923–2007

Paul J. Leibson 1952–2007 - p1013

Hans Schreiber & Vinay Kumar

doi:10.1038/ni1007-1013

Full Text - Paul J. Leibson 1952–2007 | PDF (75 KB) - Paul J. Leibson 1952–2007

One cell–one antibody: prelude and aftermath - pp1015 - 1017

G J V Nossal

doi:10.1038/ni1007-1015

Full Text - One cell–one antibody: prelude and aftermath | PDF (184 KB) - One cell–one antibody: prelude and aftermath

The clonal selection theory: 50 years since the revolution - pp1019 - 1026

Philip D Hodgkin, William R Heath & Alan G Baxter

doi:10.1038/ni1007-1019

Full Text - The clonal selection theory: 50 years since the revolution | PDF (1,875 KB) - The clonal selection theory: 50 years since the revolution | Supplementary information

CD8⁺ T cells are kept in tune by modulating IL-7 responsiveness - pp1027 - 1028

Juan Carlos Zúñiga-Pflücker

doi:10.1038/ni1007-1027

Full Text - CD8+ T cells are kept in tune by modulating IL-7 responsiveness | PDF (331 KB) - CD8+ T cells are kept in tune by modulating IL-7 responsiveness

See also: Article by Park et al.

Oxidative burst without phagocytes: the role of respiratory proteins - pp1029 - 1031

Christian Bogdan

doi:10.1038/ni1007-1029

Full Text - Oxidative burst without phagocytes: the role of respiratory proteins | PDF (229 KB) - Oxidative burst without phagocytes: the role of respiratory proteins

See also: Article by Jiang et al.

Two in one: dual function of an invertebrate antigen receptor - pp1031 - 1033

Thomas Boehm

doi:10.1038/ni1007-1031

Full Text - Two in one: dual function of an invertebrate antigen receptor | PDF (263 KB) - Two in one: dual function of an invertebrate antigen receptor

T cell receptors get back to basics - pp1033 - 1035

E Yvonne Jones, Mariolina Salio & Vincenzo Cerundolo

doi:10.1038/ni1007-1033

Full Text - T cell receptors get back to basics | PDF (605 KB) - T cell receptors get back to basics

See also: Article by Scott-Browne et al.

A catch to integrin activation - pp1035 - 1037

Rodger P McEver & Cheng Zhu

doi:10.1038/ni1007-1035

Full Text - A catch to integrin activation | PDF (715 KB) - A catch to integrin activation

See also: Article by Woolf et al.

Research Highlights - p1039

doi:10.1038/ni1007-1039

Full Text - Research Highlights | PDF (73 KB) - Research Highlights

Recent advances in antigen processing and presentation - pp1041 - 1048

Peter E Jensen

doi:10.1038/ni1516

Abstract - Recent advances in antigen processing and presentation | Full Text - Recent advances in antigen processing and presentation | PDF (564 KB) - Recent advances in antigen processing and presentation

'Coreceptor tuning': cytokine signals transcriptionally tailor CD8 coreceptor expression to the self-specificity of the TCR - pp1049 - 1059

Jung-Hyun Park, Stanley Adoro, Philip J Lucas, Sophia D Sarafova, Amala S Alag, Loretta L Doan, Batu Erman, Xiaolong Liu, Wilfried Ellmeier, Remy Bosselut, Lionel Feigenbaum & Alfred Singer

doi:10.1038/ni1512

Abstract - 'Coreceptor tuning': cytokine signals transcriptionally tailor CD8 coreceptor expression to the self-specificity of the TCR | Full Text - 'Coreceptor tuning': cytokine signals transcriptionally tailor CD8 coreceptor expression to the self-specificity of the TCR | PDF (440 KB) - 'Coreceptor tuning': cytokine signals transcriptionally tailor CD8 coreceptor expression to the self-specificity of the TCR | Supplementary information

See also: News and Views by Zúñiga-Pflücker

Minimal activation of memory CD8⁺ T cell by tissue-derived dendritic cells favors the stimulation of naive CD8⁺ T cells - pp1060 - 1066

Gabrielle T Belz, Sammy Bedoui, Fiona Kupresanin, Francis R Carbone & William R Heath

doi:10.1038/ni1505

Abstract - Minimal activation of memory CD8: +: T cell by tissue-derived dendritic cells favors the stimulation of naive CD8: +: T cells | Full Text - Minimal activation of memory CD8+ T cell by tissue-derived dendritic cells favors the stimulation of naive CD8+ T cells | PDF (346 KB) - Minimal activation of memory CD8+ T cell by tissue-derived dendritic cells favors the stimulation of naive CD8+ T cells | Supplementary information

T helper type 2 differentiation and intracellular trafficking of the interleukin 4 receptor- subunit controlled by the Rac activator Dock2 - pp1067 - 1075

Yoshihiko Tanaka, Shinjiro Hamano, Kazuhito Gotoh, Yuzo Murata, Yuya Kunisaki, Akihiko Nishikimi, Ryosuke Takii, Makiko Kawaguchi, Ayumi Inayoshi, Sadahiko Masuko, Kunisuke Himeno, Takehiko Sasazuki & Yoshinori Fukui

doi:10.1038/ni1506

Abstract - T helper type 2 differentiation and intracellular trafficking of the interleukin 4 receptor-[alpha] subunit controlled by the Rac activator Dock2 | Full Text - T helper type 2 differentiation and intracellular trafficking of the interleukin 4 receptor- subunit controlled by the Rac activator Dock2 | PDF (542 KB) - T helper type 2 differentiation and intracellular trafficking of the interleukin 4 receptor- subunit controlled by the Rac activator Dock2 | Supplementary information

Lymph node chemokines promote sustained T lymphocyte motility without triggering stable integrin adhesiveness in the absence of shear forces - pp1076 - 1085

Eilon Woolf, Irina Grigorova, Adi Sagiv, Valentin Grabovsky, Sara W Feigelson, Ziv Shulman, Tanja Hartmann, Michael Sixt, Jason G Cyster & Ronen Alon

doi:10.1038/ni1499

Abstract - Lymph node chemokines promote sustained T lymphocyte motility without triggering stable integrin adhesiveness in the absence of shear forces | Full Text - Lymph node chemokines promote sustained T lymphocyte motility without triggering stable integrin adhesiveness in the absence of shear forces | PDF (447 KB) - Lymph node chemokines promote sustained T lymphocyte motility without triggering stable integrin adhesiveness in the absence of shear forces | Supplementary information

See also: News and Views by McEver & Zhu

Lamina propria macrophages and dendritic cells differentially induce regulatory and interleukin 17–producing T cell responses - pp1086 - 1094

Timothy L Denning, Yi-chong Wang, Seema R Patel, Ifor R Williams & Bali Pulendran

doi:10.1038/ni1511

Abstract - Lamina propria macrophages and dendritic cells differentially induce regulatory and interleukin 17-producing T cell responses | Full Text - Lamina propria macrophages and dendritic cells differentially induce regulatory and interleukin 17–producing T cell responses | PDF (731 KB) - Lamina propria macrophages and dendritic cells differentially induce regulatory and interleukin 17–producing T cell responses | Supplementary information

Mast cell–derived interleukin 10 limits skin pathology in contact dermatitis and chronic irradiation with ultraviolet B - pp1095 - 1104

Michele A Grimbaldeston, Susumu Nakae, Janet Kalesnikoff, Mindy Tsai & Stephen J Galli

doi:10.1038/ni1503

Abstract - Mast cell-derived interleukin 10 limits skin pathology in contact dermatitis and chronic irradiation with ultraviolet B | Full Text - Mast cell–derived interleukin 10 limits skin pathology in contact dermatitis and chronic irradiation with ultraviolet B | PDF (787 KB) - Mast cell–derived interleukin 10 limits skin pathology in contact dermatitis and chronic irradiation with ultraviolet B | Supplementary information

Germline-encoded recognition of diverse glycolipids by natural killer T cells - pp1105 - 1113

James P Scott-Browne, Jennifer L Matsuda, Thierry Mallevaey, Janice White, Natalie A Borg, James McCluskey, Jamie Rossjohn, John Kappler, Philippa Marrack & Laurent Gapin

doi:10.1038/ni1510

Abstract - Germline-encoded recognition of diverse glycolipids by natural killer T cells | Full Text - Germline-encoded recognition of diverse glycolipids by natural killer T cells | PDF (370 KB) - Germline-encoded recognition of diverse glycolipids by natural killer T cells | Supplementary information

See also: News and Views by Jones et al.

Respiratory protein–generated reactive oxygen species as an antimicrobial strategy - pp1114 - 1122

Naxin Jiang, Nguan Soon Tan, Bow Ho & Jeak Ling Ding

doi:10.1038/ni1501

Abstract - Respiratory protein-generated reactive oxygen species as an antimicrobial strategy | Full Text - Respiratory protein–generated reactive oxygen species as an antimicrobial strategy | PDF (297 KB) - Respiratory protein–generated reactive oxygen species as an antimicrobial strategy | Supplementary information

See also: News and Views by Bogdan

Catecholaminergic neurotransmitters regulate migration and repopulation of immature human CD34⁺ cells through Wnt signaling - pp1123 - 1131

Asaf Spiegel, Shoham Shivtiel, Alexander Kalinkovich, Aya Ludin, Neta Netzer, Polina Goichberg, Yaara Azaria, Igor Resnick, Izhar Hardan, Herzel Ben-Hur, Arnon Nagler, Menachem Rubinstein & Tsvee Lapidot

doi:10.1038/ni1509

Abstract - Catecholaminergic neurotransmitters regulate migration and repopulation of immature human CD34: +: cells through : : Wnt: : signaling | Full Text - Catecholaminergic neurotransmitters regulate migration and repopulation of immature human CD34+ cells through Wnt signaling | PDF (386 KB) - Catecholaminergic neurotransmitters regulate migration and repopulation of immature human CD34+ cells through Wnt signaling

Genotoxic stress regulates expression of the proto-oncogene Bcl6 in germinal center B cells - pp1132 - 1139

Ryan T Phan, Masumichi Saito, Yukiko Kitagawa, Anthony R Means & Riccardo Dalla-Favera

doi:10.1038/ni1508

Abstract - Genotoxic stress regulates expression of the proto-oncogene : Bcl6: in germinal center B cells | Full Text - Genotoxic stress regulates expression of the proto-oncogene Bcl6 in germinal center B cells | PDF (396 KB) - Genotoxic stress regulates expression of the proto-oncogene Bcl6 in germinal center B cells | Supplementary information