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Journal articles on the topic 'Interferon-γ'

Author: Grafiati

Published: 4 June 2021

Last updated: 26 July 2025

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1

&NA;. "Interferon γ". Reactions Weekly &NA;, № 1305 (2010): 19. http://dx.doi.org/10.2165/00128415-201013050-00062.

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2

Maeyer, Edward De, та Jaqueline De Maeyer-Guignard. "Interferon-γ". Current Biology 2, № 7 (1992): 386. http://dx.doi.org/10.1016/0960-9822(92)90087-q.

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3

De Maeyer, E. "Interferon-γ". Current Opinion in Immunology 4, № 3 (1992): 321–26. http://dx.doi.org/10.1016/0952-7915(92)90083-q.

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4

Balasubramanian, Vandana, Linh T. Nguyen, Sathyamangalam V. Balasubramanian та Murali Ramanathan. "Interferon-γ-Inhibitory Oligodeoxynucleotides Alter the Conformation of Interferon-γ". Molecular Pharmacology 53, № 5 (1998): 926–32. https://doi.org/10.1016/s0026-895x(24)13260-9.

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5

Okamoto, Masakazu, Tsutomu Kawabe, Yasumasa Iwasaki та ін. "Evaluation of interferon-γ, interferon-γ-inducing cytokines, and interferon-γ–inducible chemokines in tuberculous pleural effusions". Journal of Laboratory and Clinical Medicine 145, № 2 (2005): 88–93. http://dx.doi.org/10.1016/j.lab.2004.11.013.

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6

Le-Thi-Phuong, Thao, Gaëtan Thirion, and Jean-Paul Coutelier. "Distinct gamma interferon-production pathways in mice infected with lactate dehydrogenase-elevating virus." Journal of General Virology 88, no. 11 (2007): 3063–66. http://dx.doi.org/10.1099/vir.0.83242-0.

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Two distinct pathways of gamma interferon (IFN-γ) production have been found in mice infected with lactate dehydrogenase-elevating virus. Both pathways involve natural killer cells. The first is mostly interleukin-12-independent and is not controlled by type I interferons. The second, which is suppressed by type I interferons, leads to increased levels of IFN-γ production and requires the secretion of interleukin-12. This regulation of IFN-γ production by type I interferons may help to control indirect pathogenesis induced by this cytokine.

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7

Watanabe, T., S. Fuchimoto, N. Matsubara, H. Iwagaki та K. Orita. "Anti-Proliferative Effect on Human Pancreatic Cancer Cells of Natural Human Tumour Necrosis Factor-β Combined with Natural Human Interferon-α or Interferon-γ". Journal of International Medical Research 20, № 2 (1992): 112–20. http://dx.doi.org/10.1177/030006059202000203.

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The anti-proliferative effects of natural cytokines, human tumour necrosis factor-β, natural human interferon-α and natural human interferon-γ, on three human pancreatic cancer cell lines (PANC-1, MIA PaCa-2 and BxPC-3) were investigated in vitro. The anti-proliferative effect was determined using the dye uptake method and analysed for synergism by the median effect principle. Tumour necrosis factor-β, as a single agent, had little anti-proliferative effect on any of the three cell lines, whereas interferon-α and interferon-γ exhibited a strong anti-proliferative effect against two cell lines

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Penrose, Harrison M., Akemi Katsurada, Kayoko Miyata, Maki Urushihara та Ryousuke Satou. "STAT1 regulates interferon-γ-induced angiotensinogen and MCP-1 expression in a bidirectional manner in primary cultured mesangial cells". Journal of the Renin-Angiotensin-Aldosterone System 21, № 3 (2020): 147032032094652. http://dx.doi.org/10.1177/1470320320946527.

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Objective: Intrarenal interferon-γ significantly contributes to the development of glomerular injury in which angiotensinogen and monocyte chemoattractant protein 1 levels are elevated. However, the exact nature of the role that interferon-γ plays in regulating angiotensinogen and monocyte chemoattractant protein 1 expression has not been fully delineated. Therefore, the aim of this study was to investigate the role that interferon-γ plays in angiotensinogen and monocyte chemoattractant protein 1 expression. Methods: Primary cultured rat mesangial cells were treated with 0–20 ng/mL interferon-

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9

Billiau, A. "Interferon-γ in autoimmunity". Cytokine & Growth Factor Reviews 7, № 1 (1996): 25–34. http://dx.doi.org/10.1016/1359-6101(96)00004-4.

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10

Milstone, Leonard M. "Interferon- γ Release Assay". Archives of Dermatology 148, № 1 (2012): 133. http://dx.doi.org/10.1001/archdermatol.2011.2077.

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11

Gaillard, A., та G. Dervieux. "Interferon γ — Imukin®". Lyon Pharmaceutique 46, № 1 (1995): 37–39. https://doi.org/10.1016/0024-7804(96)85714-9.

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12

Paulesu, Luana, Roberta Romagnoli, Marcella Cintorino, M. Grazia Ricci та Gianni Garotta. "First trimester human trophoblast expresses both interferon-γ and interferon-γ-receptor". Journal of Reproductive Immunology 27, № 1 (1994): 37–48. http://dx.doi.org/10.1016/0165-0378(94)90013-2.

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13

Scheglovitova, O. N., N. N. Sklyankina, N. V. Boldyreva, A. A. Babayants, I. S. Frolova, and M. R. Kapkaeva. "HUMAN INTERFERON MODULATES INFECTED VASCULAR ENDOTHELIUM FUNCTION." Annals of the Russian academy of medical sciences 69, no. 3-4 (2015): 31–35. http://dx.doi.org/10.15690/vramn.v69.i3-4.992.

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Background: To study impact of interferon (IFN) α, β and γ on the Herpes simplex virus type 1 (HSV-1) infected endothelial cells functional activity related with participation in the inflammation development. Materials and methods: In the work endothelial cells isolated from umbilical vein were used. Intact and infected cultures were treated by interferon and in the dynamics of cultivation tested mediators in the cultural medium. Results: All investigated interferons activated the production of IL-6. IFN α, β activated the production of IL-8, while IFN γ inhibited her. IFN α and γ increased sy

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14

Wang, Qixue, Xingzhe Ma, Yuanli Chen та ін. "Identification of interferon-γ as a new molecular target of liver X receptor". Biochemical Journal 459, № 2 (2014): 345–54. http://dx.doi.org/10.1042/bj20131442.

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Activation of LXR (liver X receptor) induces interferon-γ expression both in vitro and in vivo. LXR inhibits tumour growth in wild-type mice, but not in interferon-γ-knockout mice, suggesting the critical role for interferon-γ expression in LXR-inhibited tumours.

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15

Sadir, Rabia, Eric Forest та Hugues Lortat-Jacob. "The Heparan Sulfate Binding Sequence of Interferon-γ Increased the On Rate of the Interferon-γ-Interferon-γ Receptor Complex Formation". Journal of Biological Chemistry 273, № 18 (1998): 10919–25. http://dx.doi.org/10.1074/jbc.273.18.10919.

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16

Zhang, Yu-xiang, Yang Li, Yong Wang та ін. "Prospective cohort study on the clinical significance of interferon-γ, D-dimer, LDH, and CRP tests in children with severe mycoplasma pneumonia". Medicine 103, № 41 (2024): e39665. http://dx.doi.org/10.1097/md.0000000000039665.

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Background: Mycoplasma pneumoniae is a significant cause of respiratory infections in children, often leading to severe pneumonia. This study aimed to assess the clinical relevance of interferon-gamma (interferon-γ), D-dimer, lactate dehydrogenase (LDH), and C-reactive protein (CRP) as biomarkers in the severity of mycoplasma pneumonia in pediatric patients. Methods: In this prospective study, 203 pediatric patients with mycoplasma pneumonia were classified into mild (123 patients) and severe (80 patients) groups. Biomarkers including interferon-γ, D-dimer, LDH, and CRP were measured and analy

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17

Hand, Anne, Katarina Pelin, Maija Halme та ін. "Interferon-α and interferon-γ combined with chemotherapy". Anti-Cancer Drugs 4, № 3 (1993): 365–68. http://dx.doi.org/10.1097/00001813-199306000-00013.

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18

Galietta, Luis J. V., Chiara Folli, Carla Marchetti та ін. "Modification of transepithelial ion transport in human cultured bronchial epithelial cells by interferon-γ". American Journal of Physiology-Lung Cellular and Molecular Physiology 278, № 6 (2000): L1186—L1194. http://dx.doi.org/10.1152/ajplung.2000.278.6.l1186.

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Human bronchial epithelial cells were treated in vitro with interferon-γ or tumor necrosis factor-α to assess their effect on transepithelial ion transport. Short-circuit current measurements revealed that Na+absorption was markedly inhibited by interferon-γ (10–1,000 U/ml). The cystic fibrosis transmembrane conductance regulator was also downregulated by interferon-γ as evident at the protein level and by the decrease in the cAMP-dependent current. On the other hand, interferon-γ caused an increase of the current elicited by apical UTP application, which is due to the activity of Ca2+-depende

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19

CAPOBIANCHI, M. R., P. MATTANA та F. DIANZANI. "Potentiation of Interferon-αIn VitroAntiviral Activity by Interferon-γ Is Not Abrogated by Antibody to Interferon-γ". Journal of Interferon Research 13, № 1 (1993): 53–55. http://dx.doi.org/10.1089/jir.1993.13.53.

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20

Zhao, Yunjuan, Yunliang Xie та Wangen Li. "Liraglutide Exerts Potential Anti-inflammatory Effect in Type 1 Diabetes by Inhibiting IFN-γ Production via Suppressing JAK-STAT Pathway". Endocrine, Metabolic & Immune Disorders - Drug Targets 19, № 5 (2019): 656–64. http://dx.doi.org/10.2174/1871530319666190301115654.

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Background: Type 1 diabetes is a T cell-mediated autoimmune disease. Interferon γ plays a critical role in the pathogenesis of type 1 diabetes. Signal transducer and activator of transcription transduces type I interferon cytokines in T cells, leading to Th1 cell differentiation and production of interferon γ. Recent studies suggest that liraglutide reduces the plasma concentration of C-reative protein in patients with type 1 diabetes and protects β cell function in the non-obese diabetic mouse. Objective: The study aimed to explore the effect of glucagon-like peptide-1 analogue on interferon

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21

Barkhouse, Darryll A., Samantha A. Garcia, Emily K. Bongiorno, Aurore Lebrun, Milosz Faber, and D. Craig Hooper. "Expression of Interferon Gamma by a Recombinant Rabies Virus Strongly Attenuates the Pathogenicity of the Virus via Induction of Type I Interferon." Journal of Virology 89, no. 1 (2014): 312–22. http://dx.doi.org/10.1128/jvi.01572-14.

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ABSTRACTPrevious animal model experiments have shown a correlation between interferon gamma (IFN-γ) expression and both survival from infection with attenuated rabies virus (RABV) and reduction of neurological sequelae. Therefore, we hypothesized that rapid production of murine IFN-γ by the rabies virus itself would induce a more robust antiviral response than would occur naturally in mice. To test this hypothesis, we used reverse engineering to clone the mouse IFN-γ gene into a pathogenic rabies virus backbone, SPBN, to produce the recombinant rabies virus designated SPBNγ. Morbidity and mort

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22

Chkhenkeli, V. A. "Veterinary drug Trametin obtained on the basis of <i>Trametes pubescens</i> xylotroph fungi: its effect on the biosynthesis of interferons and its prophylactic activity against calf respiratory diseases." Proceedings of Universities. Applied Chemistry and Biotechnology 11, no. 4 (2022): 581–89. http://dx.doi.org/10.21285/2227-2925-2021-11-4-581-589.

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Given the spread of bacterial and viral diseases in young farm animals, the use of interferons and drugs to stimulate their biosynthesis has gained relevance. In a previous study, we examined the effect of a veterinary drug Trametin produced on the basis of Trametes pubescens (Shumach.: Fr.) Pilat. on the biosynthesis of interferons in the blood of mice. The present work is aimed at studying the biosynthesis dynamics of α- and γ-interferons when using Trametin and studying its prophylactic activity in calves. It is shown that a single oral administration of Trametin in doses ranging from 15 to

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23

Wipasa, Jiraprapa, Romanee Chaiwarith, Kriangkrai Chawansuntati, Jutarat Praparattanapan, Kritsadee Rattanathammethee та Khuanchai Supparatpinyo. "Characterization of anti-interferon-γ antibodies in HIV-negative immunodeficient patients infected with unusual intracellular microorganisms". Experimental Biology and Medicine 243, № 7 (2018): 621–26. http://dx.doi.org/10.1177/1535370218764086.

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A major characteristic of immunodeficiency associated with life-threatening intracellular infection in adults is the presence of anti-interferon-γ antibodies. Although little is known about the mechanism underlying this syndrome, it is believed that the antibodies inhibit the activity of downstream signaling pathway of interferon-γ. In this study, the characteristics of these antibodies in patients who presented, or have a history of, intracellular infection and were positive to anti-interferon-γ antibodies were investigated. The antibodies exhibited mainly the IgG1 and the IgG4 subtypes and r

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24

Kalalo, Lina, Diana Takumansang-Sondakh, and Audrey Wahani. "Cotinine and interferon-gamma levels in pre-school children exposed to household tobacco smoke." Paediatrica Indonesiana 53, no. 5 (2016): 287. http://dx.doi.org/10.14238/pi53.5.2013.287-90.

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Background Environmental tobacco smoke has been consistently linked to negative health outcomes, especially in children, including an increased susceptibility to infections. Cigarette smoking has a depressive effect on interferon-γ (IFN-γ). Serum cotinine is a marker of exposure to smoke.Objective To determine the association between serum cotinine and interferon-γ (IFN-γ) levels in children with household tobacco smoke exposure.Methods We conducted a cross-sectional study at the Tumumpa and Singkil Districts of Manado, Indonesia, from February to May 2012. Subjects were collected by consecuti

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25

Geraghty, Patrick, Catherine M. Greene, Michael O'Mahony, Shane J. O'Neill, Clifford C. Taggart та Noel G. McElvaney. "Secretory Leucocyte Protease Inhibitor Inhibits Interferon-γ-induced Cathepsin S Expression". Journal of Biological Chemistry 282, № 46 (2007): 33389–95. http://dx.doi.org/10.1074/jbc.m706884200.

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We have demonstrated that bronchoalveolar lavage fluid from chronic obstructive pulmonary disease patients contains higher levels of interferon-γ compared with controls. Interferon-γ is a potent inducer of various cathepsins and matrix metalloproteases. Therefore, we postulated that interferon-γ could induce protease expression by macrophages in acute and chronic lung disease. Chronic obstructive pulmonary disease patients had greater levels of cathepsin S and matrix metalloprotease-12 in their bronchoalveolar lavage fluid. Macrophages incubated with chronic obstructive pulmonary disease bronc

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26

Sanderson, Nicholas, Mariana Puntel, Kurt Kroeger та ін. "Immunological synapses do not restrict secretion of interferon γ during antigen-specific lysis of target cells by CD-8+ cytotoxic T lymphocytes (48.12)". Journal of Immunology 186, № 1_Supplement (2011): 48.12. http://dx.doi.org/10.4049/jimmunol.186.supp.48.12.

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Abstract Cytotoxic T lymphocytes display two main effector mechanisms when interacting with target cells in an antigen-specific manner: (i) destruction of the target cell, and (ii) secretion of cytokines. It is thought that while target cell lysis occurs following brief contact with the T cell, cytokine secretion requires formation of immunological synapses between T cells and target cells. At immunological synapses between CTLs and adenovirus-infected astrocytes in the brain, interferon γ is polarized at the contact, suggesting immunological synapses constrain secretion of interferon γ. To te

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27

O'Sullivan, M. G., L. N. Fleisher, N. C. Olson, N. J. MacLachlan, and T. T. Brown. "Modulation of arachidonic acid metabolism by bovine alveolar macrophages exposed to interferons and lipopolysaccharide." American Journal of Veterinary Research 51, no. 11 (1990): 1820–25. http://dx.doi.org/10.2460/ajvr.1990.51.11.1820.

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SUMMARY Stimulation of bovine alveolar macrophages with calcium ionophore A23187 resulted in marked production of leukotriene (lt)B4 and a lesser increase in thromboxane (tx)B2, whereas opsonized zymosan (opz) resulted in production of txb2 and relatively small increases in ltb4 and prostaglandin (pg)F2α. Alveolar macrophages incubated with recombinant bovine interferon-γ or lipopolysaccharide, and subsequently stimulated with A23187 or opz, had altered arachidonic acid metabolism, producing markedly increased amounts of txb2 and pgf2α, and slightly increased ltb4. Incubation of alveolar macro

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28

Tsuji, Kohichiro, Kenji Muraoka та Tatsutoshi Nakahata. "Interferon-γ and Human Megakaryopoiesis". Leukemia & Lymphoma 31, № 1-2 (1998): 107–13. http://dx.doi.org/10.3109/10428199809057590.

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29

Palumbo, Antonio, Benedetto Bruno, Mario Boccadoro та Alessandro Pileri. "Interferon-γ in Multiple Myeloma". Leukemia & Lymphoma 18, № 3-4 (1995): 215–19. http://dx.doi.org/10.3109/10428199509059610.

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30

Dries, David J., та John F. Perry. "Interferon-γ: Titration of inflammation *". Critical Care Medicine 30, № 7 (2002): 1663–64. http://dx.doi.org/10.1097/00003246-200207000-00050.

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31

Stevens, David A., Elmer Brummer та Karl V. Clemons. "Interferon‐γ as an Antifungal". Journal of Infectious Diseases 194, s1 (2006): S33—S37. http://dx.doi.org/10.1086/505357.

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32

Welberg, Leonie. "Interferon-γ tunes the rhythm". Nature Reviews Neuroscience 13, № 2 (2012): 74–75. http://dx.doi.org/10.1038/nrn3177.

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33

Rose, Marlene L. "Interferon-γ and Intimal Hyperplasia". Circulation Research 101, № 6 (2007): 542–44. http://dx.doi.org/10.1161/circresaha.107.160911.

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34

Pai, Madhukar, та David M. Lewinsohn. "Interferon-γ Assays for Tuberculosis". American Journal of Respiratory and Critical Care Medicine 172, № 5 (2005): 519–21. http://dx.doi.org/10.1164/rccm.2506003.

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35

Landolfo, S., та G. Cavallo. "Interferon γ: An immunological slant". Annales de l'Institut Pasteur / Immunologie 136, № 1 (1985): 84–91. http://dx.doi.org/10.1016/s0769-2625(85)80082-9.

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36

Smith-Jones, Peter M., Werner Linkesch та Irene Virgolini. "Interferon-γ for respiratory diseases". Lancet 350, № 9076 (1997): 524. http://dx.doi.org/10.1016/s0140-6736(05)63124-8.

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37

Boehm, U., T. Klamp, M. Groot та J. C. Howard. "CELLULAR RESPONSES TO INTERFERON-γ". Annual Review of Immunology 15, № 1 (1997): 749–95. http://dx.doi.org/10.1146/annurev.immunol.15.1.749.

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38

Priwitzer, M., C. Unger, F. Spieth та G. Klittich. "Falsch-positiver Interferon-γ-Test?" Pneumologie 61, № 3 (2007): 157–58. http://dx.doi.org/10.1055/s-2006-954980.

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39

Miller, Catriona H. T., Stephen G. Maher та Howard A. Young. "Clinical Use of Interferon-γ". Annals of the New York Academy of Sciences 1182, № 1 (2009): 69–79. http://dx.doi.org/10.1111/j.1749-6632.2009.05069.x.

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40

Dunn, Gavin P., Hiroaki Ikeda, Allen T. Bruce та ін. "Interferon-γ and Cancer Immunoediting". Immunologic Research 32, № 1-3 (2005): 231–46. http://dx.doi.org/10.1385/ir:32:1-3:231.

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41

Diel, R., та A. Nienhaus. "Interferon-γ Release Assays (IGRA)". Der Pneumologe 8, № 3 (2011): 162–67. http://dx.doi.org/10.1007/s10405-010-0406-1.

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42

Billiau, Alfons, та Patrick Matthys. "Interferon-γ: A historical perspective". Cytokine & Growth Factor Reviews 20, № 2 (2009): 97–113. http://dx.doi.org/10.1016/j.cytogfr.2009.02.004.

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43

Ilyushin, A. L., I. V. Bogdashin, A. Z. Aleksanyan, V. V. Novikov та L. A. Ashrafyan. "Interferon-γ and tumor growth". Siberian journal of oncology 22, № 4 (2023): 118–27. http://dx.doi.org/10.21294/1814-4861-2023-22-4-118-127.

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Purpose of the study: to analyze published data on the mechanisms of action of interferon gamma (IFN-γ) in tumor growth and to evaluate the possibility of its use in the treatment of solid tumors. Material and Methods. More than 200 publications were found in the Scopus, Pubmed, eLibrary and other databases, the search keywords were: interferon gamma, tumor growth, cancer therapy. This review includes 54 papers. Results. IFN-γ is a pleiotropic cytokine with antiviral, antitumor, and immunomodulatory functions and plays an important role in coordinating the innate and adaptive immune response.

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PRÜMMER, OTTO, CHRISTOPH FIEHN та HARALD GALLATI. "Anti-Interferon-γ Antibodies in a Patient Undergoing Interferon-γ Treatment for Systemic Mastocytosis". Journal of Interferon & Cytokine Research 16, № 7 (1996): 519–22. http://dx.doi.org/10.1089/jir.1996.16.519.

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45

Fountoulakis, M., E. Takacsdilorenzo, J. F. Juranville та M. Manneberg. "Purification of Interferon γ-Interferon γ Receptor Complexes by Preparative Electrophoresis on Native Gels". Analytical Biochemistry 208, № 2 (1993): 270–76. http://dx.doi.org/10.1006/abio.1993.1045.

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46

Burn, Thomas N., Lehn Weaver, Julia E. Rood та ін. "Genetic Deficiency of Interferon‐γ Reveals Interferon‐γ–Independent Manifestations of Murine Hemophagocytic Lymphohistiocytosis". Arthritis & Rheumatology 72, № 2 (2019): 335–47. http://dx.doi.org/10.1002/art.41076.

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47

CHEN, Li-Chun, Diane KEPKA-LENHART, Timothy M. WRIGHT та Sidney M. MORRIS. "Salicylate-enhanced activation of transcription factors induced by interferon-γ". Biochemical Journal 342, № 3 (1999): 503–7. http://dx.doi.org/10.1042/bj3420503.

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Salicylate enhanced the interferon-γ-dependent activation of two transcription factors in a murine macrophage cell line: signal transducer and activator of transcription (STAT)1 and interferon-γ-responsive factor 1. Salicylate alone did not activate these transcription factors. This enhancement was reflected by increased DNA-binding activities and was the consequence of prolonged tyrosine phosphorylation of these transcription factors following interferon-γ treatment. However, salicylate did not directly inhibit protein-tyrosine phosphatase activity in nuclear extracts of interferon-γ-treated

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48

Filipič, Bratko, Klemen Rihar, Dunja Exel Gregorič та ін. "Enhancing Effect of 100.414-kHz Electromagnetic Field Produced by Defender’s Pulse Generator on the ChIFN γ-Like Molecule Inducing Capacity of Lens culinaris Agglutinin and 10% PBS Washouts of Different Holocene Minerals". Technology in Cancer Research & Treatment 18 (1 січня 2019): 153303381882109. http://dx.doi.org/10.1177/1533033818821093.

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Macrophages play key role in host defense and tissue repair, and thus understanding regulation of their function is important. For instance, our previous results have shown that in chicken macrophage system (CoMA cell line), application of a pulse of electromagnetic fields of frequencies 0.618, 1.054, 5.229, and 100.414 kHz induces production of interferon γ-like molecules. In this study, we have shown that the electromagnetic field of 100.414 kHz is the most effective in inducing synthesis of chicken interferon γ and chicken interferon γ-like molecules in CoMA cells, especially when combined

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49

Gu, Wenyi, Jiezhong Chen, Lei Yang та Kong-Nan Zhao. "TNF-αPromotes IFN-γ-Induced CD40 Expression and Antigen Process in Myb-Transformed Hematological Cells". Scientific World Journal 2012 (2012): 1–11. http://dx.doi.org/10.1100/2012/621969.

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Tumour necrosis factor-α, interferon-γand interleukin-4 are critical cytokines in regulating the immune responses against infections and tumours. In this study, we investigated the effects of three cytokines on CD40 expression in Myb-transformed hematological cells and their regulatory roles in promoting these cells into dendritic cells. We observed that both interleukin-4 and interferon-γincreased CD40 expression in these hematological cells in a dose-dependent manner, although the concentration required for interleukin-4 was significantly higher than that for interferon-γ. We found that tumo

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50

Peng, Tao, Jia Zhu, Yon Hwangbo, Lawrence Corey, and Roger E. Bumgarner. "Independent and Cooperative Antiviral Actions of Beta Interferon and Gamma Interferon against Herpes Simplex Virus Replication in Primary Human Fibroblasts." Journal of Virology 82, no. 4 (2007): 1934–45. http://dx.doi.org/10.1128/jvi.01649-07.

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ABSTRACT Type I and type II interferons (IFNs) act in synergy to inhibit the replication of a variety of viruses, including herpes simplex virus (HSV). To understand the mechanism of this effect, we have analyzed the transcriptional profiles of primary human fibroblast cells that were first treated with IFN-β1, IFN-γ, or a combination of both and then subsequently infected with HSV-1. We have identified two types of synergistic activities in the gene expression patterns induced by IFN-β1 and IFN-γ that may contribute to inhibition of HSV-1 replication. The first is defined as “synergy by indep

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