Document Information


PMID 18246426  (  )
Title Elevated inflammatory markers in a group of amyotrophic lateral sclerosis patients from northern India.
Abstract The role of cytokines in the pathophysiology of amyotrophic lateral sclerosis (ALS) and its relation to clinical outcome has not been clearly defined. We evaluated tumor necrosis factor-alpha (TNF-alpha), interferon-gamma (IFN-gamma) and nitric oxide (NO) levels in the serum of 22 ALS patients and 20 controls. Serum TNF-alpha levels and IFN-gamma levels were significantly (P < 0.001) elevated in ALS patients. We also observed NO levels to be significantly (P < 0.05) increased with respect to normal subjects. We further noticed positive correlation between the duration of ALS and these proinflammatory molecule levels. Exitotoxicity and oxidative stress are known to play a crucial role in the neurodegeneration observed in ALS. Since high levels of TNF-alpha are known to be cytotoxic, it could be that a complex interplay of these effectors may be one of the factors underlying the progression of ALS. This study confirms the involvement of inflammation in ALS and the need to develop surrogate markers to check the progression of this disease. Sciences, Raebareli Road, Lucknow, UP 226014, India. gnageshbabu@yahoo.com

NOTE: Color highlight is limited to the abstract and SciMiner text-mining mode. If you see much more identified targets below from "Targets by SciMiner Summary" and "Targets by SciMiner Full list", they may have been identified from the full text.



Targets by SciMiner Summary

HUGO ID Symbol Target Name #Occur ActualStr
11892TNFtumor necrosis factor (TNF superfamily, member 2)28tumor necrosis factor | tumor necrosis factor alpha | TNF-A |
5438IFNGinterferon, gamma20IFN-G |
7872NOS1nitric oxide synthase 1 (neuronal)5NOS | nNOS |
6018IL6interleukin 6 (interferon, beta 2)4IL-6 | il 6 |
7873NOS2Anitric oxide synthase 2A (inducible, hepatocytes)2iNOS | nitric oxide synthase |
6925MBPmyelin basic protein1myelin basic protein |

 


Targets by SciMiner Full list

HUGO ID Symbol Name ActualStr Score FlankingText
11892TNFtumor necrosis factor (TNF superfamily, member 2)TNF-A1.7We evaluated tumor necrosis factor-alpha (TNF-A), TNF-A interferon-G (IFN-G) IFN-G and nitric oxide (NO) NO levels in
5438IFNGinterferon, gammaIFN-G0.8We evaluated tumor necrosis factor-alpha (TNF-A), TNF-A interferon-G (IFN-G) IFN-G and nitric oxide (NO) NO levels in the serum of
11892TNFtumor necrosis factor (TNF superfamily, member 2)TNF-A1.7Serum TNF-A levels and IFN-G levels were significantly ( P _lt_ 0.001
5438IFNGinterferon, gammaIFN-G0.8Serum TNF-A levels and IFN-G levels were significantly ( P _lt_ 0.001 elevated in ALS
11892TNFtumor necrosis factor (TNF superfamily, member 2)TNF-A1.7Since high levels of TNF-A are known to be cytotoxic it could be that a
11892TNFtumor necrosis factor (TNF superfamily, member 2)TNF-A1.7role of proinflammatory cytokines such as tumor necrosis factor-A (TNF-A) TNF-A and interferon-G (IFN-G) IFN-G as potential mediators during the progression
5438IFNGinterferon, gammaIFN-G0.8such as tumor necrosis factor-A (TNF-A) TNF-A and interferon-G (IFN-G) IFN-G as potential mediators during the progression of brain injury is
11892TNFtumor necrosis factor (TNF superfamily, member 2)TNF-A1.7TNF-A is essential to orchestrate the immune response in the brain
11892TNFtumor necrosis factor (TNF superfamily, member 2)TNF-A1.7The duration of the response and levels of TNF-A in the cerebral environment may be the critical factors for
11892TNFtumor necrosis factor (TNF superfamily, member 2)TNF-A1.7The detrimental effects of TNF-A in the CNS may also depend on the presence of
11892TNFtumor necrosis factor (TNF superfamily, member 2)TNF-A1.7Ag stimulated T cells have the ability to produce TNF-A along with IFN-G that acts in both innate and specific
5438IFNGinterferon, gammaIFN-G0.8T cells have the ability to produce TNF-A along with IFN-G that acts in both innate and specific cell-mediated immunities 16
11892TNFtumor necrosis factor (TNF superfamily, member 2)TNF-A1.7The mixture of both TNF-A and IFN-G may therefore be harmful to neuronal elements
5438IFNGinterferon, gammaIFN-G0.8The mixture of both TNF-A and IFN-G may therefore be harmful to neuronal elements
5438IFNGinterferon, gammaIFN-G0.8In this regard transgenic mice expressing IFN-G in hippocampus exhibit profound enhanced microglial reactivity to lesion-induced neuronal
5438IFNGinterferon, gammaIFN-G0.8profound enhanced microglial reactivity to lesion-induced neuronal injury indicating that IFN-G acts as an amplifier of the response 17
5438IFNGinterferon, gammaIFN-G0.8Four days of treatment with IFN-G failed to alter cell survival or myelin basic protein gene
11892TNFtumor necrosis factor (TNF superfamily, member 2)TNF-A1.7Fas-mediated apoptosis and this effect is augmented in presence of TNF-A 18
7872NOS1nitric oxide synthase 1 (neuronal)NOS2.7is synthesized from l -arginine by nitric oxide synthase (NOS) NOS 22 23
7872NOS1nitric oxide synthase 1 (neuronal)NOS2.7Within the CNS two isoforms of NOS exist calcium dependent neuronal form (nNOS) nNOS and inducible calcium
7872NOS1nitric oxide synthase 1 (neuronal)nNOS2.7two isoforms of NOS exist calcium dependent neuronal form (nNOS) nNOS and inducible calcium independent form (iNOS) iNOS
7873NOS2Anitric oxide synthase 2A (inducible, hepatocytes)iNOS2.7neuronal form (nNOS) nNOS and inducible calcium independent form (iNOS) iNOS
7872NOS1nitric oxide synthase 1 (neuronal)nNOS2.7Under normal conditions neurons containing nNOS release relatively small quantities of NO which has neurotransmitter like
11892TNFtumor necrosis factor (TNF superfamily, member 2)TNF-A1.7of this study is to measure the systemic inflammatory markers TNF-A IFN-G and nitric oxide in ALS patients and evaluate their
5438IFNGinterferon, gammaIFN-G0.8this study is to measure the systemic inflammatory markers TNF-A IFN-G and nitric oxide in ALS patients and evaluate their role
11892TNFtumor necrosis factor (TNF superfamily, member 2)TNF-A1.7TNF-A and IFN-G assay The serum thus obtained was stored at
5438IFNGinterferon, gammaIFN-G0.8TNF-A and IFN-G assay The serum thus obtained was stored at _amp_#8722 80C
11892TNFtumor necrosis factor (TNF superfamily, member 2)TNF-A1.7obtained was stored at _amp_#8722 80C and was used for TNF-A and IFN-G estimation by ELISA
5438IFNGinterferon, gammaIFN-G0.8stored at _amp_#8722 80C and was used for TNF-A and IFN-G estimation by ELISA
11892TNFtumor necrosis factor (TNF superfamily, member 2)TNF-A1.7Elisa kits for the estimation of TNF-A and IFN-G were obtained from R_amp_D Systems Minneapolis MN USA
5438IFNGinterferon, gammaIFN-G0.8Elisa kits for the estimation of TNF-A and IFN-G were obtained from R_amp_D Systems Minneapolis MN USA
11892TNFtumor necrosis factor (TNF superfamily, member 2)TNF-A1.7It may be noted that serum TNF-A levels in ALS patients were significantly higher ( P _lt_
5438IFNGinterferon, gammaIFN-G0.8noticed a significant elevation ( P _lt_ 0.001 in serum IFN-G NO levels in ALS patients versus controls (Figs Figs 2
11892TNFtumor necrosis factor (TNF superfamily, member 2)TNF-A1.7Fig 1 Serum mean TNF-A (pg/ml pg ml SEM levels in ALS patients ( n
5438IFNGinterferon, gammaIFN-G0.8Fig 2 Serum mean IFN-G (pg/ml pg ml SEM levels in ALS patients ( n
11892TNFtumor necrosis factor (TNF superfamily, member 2)TNF-A1.7Furthermore it can be seen that in ALS patients serum TNF-A IFN-G and NO levels (Figs Figs 4 -6 respectively started
5438IFNGinterferon, gammaIFN-G0.8it can be seen that in ALS patients serum TNF-A IFN-G and NO levels (Figs Figs 4 -6 respectively started to
11892TNFtumor necrosis factor (TNF superfamily, member 2)TNF-A1.7Fig 4 Second degree polynomial regression plot showing serum mean TNF-A (pg/ml pg ml SEM levels versus duration of illness in
5438IFNGinterferon, gammaIFN-G0.8Fig 5 Second degree polynomial regression plot showing IFN-G levels (pg/ml pg ml SEM versus duration of illness in
6018IL6interleukin 6 (interferon, beta 2)IL-61.3a result of its anti-inflammatory action on cytokines such as IL-6
11892TNFtumor necrosis factor (TNF superfamily, member 2)TNF-A1.7In the present study we observed significant elevation in serum TNF-A and IFN-G levels in ALS patients and also this increase
5438IFNGinterferon, gammaIFN-G0.8present study we observed significant elevation in serum TNF-A and IFN-G levels in ALS patients and also this increase was most
6018IL6interleukin 6 (interferon, beta 2)IL-61.3Moreau et al 29 measured IL-6 and TNF-A in patients with ALS
11892TNFtumor necrosis factor (TNF superfamily, member 2)TNF-A1.7Moreau et al 29 measured IL-6 and TNF-A in patients with ALS
11892TNFtumor necrosis factor (TNF superfamily, member 2)TNF-A1.7none of the patients including the five patients in whom TNF-A levels peaked at 24 months were having any significant respiratory
11892TNFtumor necrosis factor (TNF superfamily, member 2)TNF-A1.7The source for the increased serum TNF-A and IFN-G in the present study could be peripheral immune
5438IFNGinterferon, gammaIFN-G0.8The source for the increased serum TNF-A and IFN-G in the present study could be peripheral immune cells
11892TNFtumor necrosis factor (TNF superfamily, member 2)TNF-A1.7et al 30 did not find any correlation between blood TNF-A levels and duration of the disease in ALS patients
11892TNFtumor necrosis factor (TNF superfamily, member 2)TNF-A1.7Moreover Holmoy et al 31 could not detect TNF-A and IFN-G levels in the CSF of ALS patients using
5438IFNGinterferon, gammaIFN-G0.8Moreover Holmoy et al 31 could not detect TNF-A and IFN-G levels in the CSF of ALS patients using a cytometric
7872NOS1nitric oxide synthase 1 (neuronal)NOS2.7Considering that NO levels correlate closely with the activity of NOS in brain 34 the pronounced increases found in ALS patients
11892TNFtumor necrosis factor (TNF superfamily, member 2)TNF-A1.7To conclude serum TNF-A and IFN-G levels peaked around 24 months from the onset
5438IFNGinterferon, gammaIFN-G0.8To conclude serum TNF-A and IFN-G levels peaked around 24 months from the onset in these
11892TNFtumor necrosis factor (TNF superfamily, member 2)tumor necrosis factor alpha1.0we evaluated tumor necrosis factor alpha tnf a interferon g ifn g and nitric oxide no levels in the serum of 22 als patients and 20 controls.
11892TNFtumor necrosis factor (TNF superfamily, member 2)tumor necrosis factor1.0keywords amyotrophic lateral sclerosis tumor necrosis factor a interferon g nitric oxide inflammation
11892TNFtumor necrosis factor (TNF superfamily, member 2)tumor necrosis factor1.0the role of proinflammatory cytokines such as tumor necrosis factor a tnf a and interferon g ifn g as potential mediators during the progression of brain injury is not clear.
6925MBPmyelin basic proteinmyelin basic protein1.0four days of treatment with ifn g failed to alter cell survival or myelin basic protein gene expression in cultured human oligodendrocytes but these cells are more susceptible to fas mediated apoptosis and this effect is augmented in presence of tnf a [ 18 ].
7873NOS2Anitric oxide synthase 2A (inducible, hepatocytes)nitric oxide synthase1.0no is synthesized from l arginine by nitric oxide synthase nos [ 22 23 ].
6018IL6interleukin 6 (interferon, beta 2)il 61.0czlonkowska et al. [ 28 ] showed that neuroprotective activity of estrogen could be partially a result of its anti inflammatory action on cytokines such as il 6.
6018IL6interleukin 6 (interferon, beta 2)il 61.0moreau et al. [ 29 ] measured il 6 and tnf a in patients with als.