36 research outputs found
NKG2A inhibits TH2 cell effector function in vitro
- Author
- AG Brooks
- Bahar Mojgani
- BC Sheu
- C Brando
- C Vitale
- E Hofer
- Eric P Hoffman
- F Borrego
- F Megret
- H Kawamura
- IY Pappworth
- J Kabat
- J Nattermann
- JD Miller
- JP Houchins
- JP Houchins
- Kanneboyina Nagaraju
- L Derre
- M Jinushi
- M Lopez-Botet
- Maryam Nazemzadeh
- MC Gold
- ML Labonte
- N Lee
- PE Posch
- RJ Freishtat
- Robert J Freishtat
- S Lazetic
- S Maier
- S Suvas
- T Yabe
- VM Braud
- VM Braud
- Publication venue
- BioMed Central
- Publication date
- 01/01/2007
- Field of study
This is an Open Access article distributed under the terms of the Creative Commons Attribution Licens
Extended LTA, TNF, LST1 and HLA Gene Haplotypes and Their Association with Rubella Vaccine-Induced Immunity
- Author
- A Lanas
- AG Wilson
- AV Hill
- Bengt Hansson
- BJ Hennig
- D
- D Mewar
- D Ou
- DJ Schaid
- GA Poland
- GA Poland
- Gregory A. Poland
- GT Nepom
- H Mulcahy
- H Rau
- I Rollinger-Holzinger
- IG Ovsyannikova
- IG Ovsyannikova
- IG Ovsyannikova
- IG Ovsyannikova
- IG Ovsyannikova
- IG Ovsyannikova
- Inna G. Ovsyannikova
- JH Robinson
- JR Bradley
- JR Kerr
- M Diakite
- MM Miretti
- NJD Nagelkerke
- PE Posch
- Robert A. Vierkant
- Robert M. Jacobson
- S Vejbaesya
- T Hohler
- T Tomoyose
- TG Kimman
- V. Shane Pankratz
- Y Yang
- Publication venue
- Public Library of Science
- Publication date
- 01/07/2010
- Field of study
Recent studies have suggested the importance of HLA genes in determining immune responses following rubella vaccine. The telomeric class III region of the HLA complex harbors several genes, including lymphotoxin alpha (LTA), tumor necrosis factor (TNF) and leukocyte specific transcript -1 (LST1) genes, located between the class I B and class II DRB1 loci. Apart from HLA, little is known about the effect of this extended genetic region on HLA haplotypic backgrounds as applied to immune responses.We examined the association between immune responses and extended class I-class II-class III haplotypes among 714 healthy children after two doses of rubella vaccination. These extended haplotypes were then compared to the HLA-only haplotypes. The most significant association was observed between haplotypes extending across the HLA class I region, ten-SNP haplotypes, and the HLA class II region (i.e. A-C-B-LTA-TNF-LST1-DRB1-DQA1-DQB1-DPA1-DPB1) and rubella-specific antibodies (global p-value of 0.03). Associations were found between both extended A*02-C*03-B*15-AAAACGGGGC-DRB1*04-DQA1*03-DQB1*03-DPA1*01-DPB1*04 (p = 0.002) and HLA-only A*02-C*03-B*15-DRB1*04-DQA1*03-DQB1*03-DPA1*01-DPB1*04 haplotypes (p = 0.009) and higher levels of rubella antibodies. The class II HLA-only haplotype DRB1*13-DQA1*01-DQB1*06-DPA1*01-DPB1*04 (p = 0.04) lacking LTA-TNF-LST1 SNPs was associated with lower rubella antibody responses. Similarly, the class I-class II HLA-only A*01-C*07-B*08-DRB1*03-DQA1*05-DQB1*02-DPA1*01-DPB1*04 haplotype was associated with increased TNF-alpha secretion levels (p = 0.009). In contrast, the extended AAAACGGGGC-DRB1*01-DQA1*01-DQB1*05-DPA1*01-DPB1*04 (p = 0.01) haplotype was found to trend with decreased rubella-specific IL-6 secretion levels.These data suggest the importance of examining both HLA genes and genes in the class III region as part of the extended haplotypes useful in understanding genomic drivers regulating immune responses to rubella vaccine
Primate TNF Promoters Reveal Markers of Phylogeny and Evolution of Innate Immunity
- Author
- A Baena
- A Fischer
- A Hamann
- A Richardson
- A Varki
- AE Goldfeld
- AE Goldfeld
- AG Wilson
- AG Wilson
- AH Hajeer
- Alan R. Mootnick
- Alla V. Tsytsykova
- AM Uglialoro
- Andres Baena
- Anne E. Goldfeld
- AR Mootnick
- AR Mootnick
- AV Tsytsykova
- AV Tsytsykova
- BM Brinkman
- C Roos
- C. Groves
- CA Alper
- CC Muir
- CG Schrago
- CG Schrago
- Christopher Arendt
- Claudia Brieva
- D Boffelli
- D Boffelli
- D Brandon-Jones
- D Hata
- DA Hinds
- DA Tagle
- DE Wildman
- DL Swofford
- E Bailes
- EC Hernández
- EH McConkey
- EJ Yunis
- EY Tsai
- EY Tsai
- EY Tsai
- F Gao
- F Heissig
- F Mérien
- F Villinger
- F Waldron-Lynch
- Filipa Ligeiro
- GM Cooper
- GV Glazko
- HC Ackerman
- HH Stedman
- I Ebersberger
- I Hellmann
- I Ovcharenko
- J Felsenstein
- J Klein
- J Wienberg
- James V. Falvo
- JC Aguillon
- JC Delgado
- JC Opazo
- JD Thompson
- JG Hacia
- JG Hacia
- JM Heraud
- JP Bayley
- JP Noonan
- JV Falvo
- JY Leung
- L Li
- L Zhi
- M Caceres
- M Goodman
- M Ruvolo
- ME Woolhouse
- MT Webster
- MV Hollegaard
- MV Olson
- MV Rockman
- MV Rockman
- MW Hahn
- MW Karaman
- N Patterson
- Oliver A. Ryder
- Ousmane M. Diop
- P Gagneux
- P Khaitovich
- PA Zimmerman
- Pascal Gagneux
- PE Posch
- R Barthel
- R Wimmer
- RA Mittermeier
- RD Allen
- RE Green
- RL Raaum
- RL Stauffer
- S D'Alfonso
- S Kumar
- S Kumar
- S Mummidi
- S Müller
- SB Carroll
- SB Carroll
- SB Haudek
- SB Haudek
- SL Page
- Stephen J. O'Brien
- T Higuchi
- W Enard
- W Enard
- W Enard
- WB Harland
- X Gao
- X Xu
- Y Gilad
- Y Gilad
- Y Zhang
- Z Takacs
- Publication venue
- NSUWorks
- Publication date
- 01/01/2007
- Field of study
Background. Tumor necrosis factor (TNF) is a critical cytokine in the immune response whose transcriptional activation is controlled by a proximal promoter region that is highly conserved in mammals and, in particular, primates. Specific single nucleotide polymorphisms (SNPs) upstream of the proximal human TNF promoter have been identified, which are markers of human ancestry.
Methodology/Principal findings. Using a comparative genomics approach we show that certain fixed genetic differences in the TNF promoter serve as markers of primate speciation. We also demonstrate that distinct alleles of most human TNF promoter SNPs are identical to fixed nucleotides in primate TNF promoters. Furthermore, we identify fixed genetic differences within the proximal TNF promoters of Asian apes that do not occur in African ape or human TNF promoters. Strikingly, protein-DNA binding assays and gene reporter assays comparing these Asian ape TNF promoters to African ape and human TNF promoters demonstrate that, unlike the fixed differences that we define that are associated with primate phylogeny, these Asian ape-specific fixed differences impair transcription factor binding at an Sp1 site and decrease TNF transcription induced by bacterial stimulation of macrophages.
Conclusions/significance. Here, we have presented the broadest interspecies comparison of a regulatory region of an innate immune response gene to date. We have characterized nucleotide positions in Asian ape TNF promoters that underlie functional changes in cell type- and stimulus-specific activation of the TNF gene. We have also identified ancestral TNF promoter nucleotide states in the primate lineage that correspond to human SNP alleles. These findings may reflect evolution of Asian and African apes under a distinct set of infectious disease pressures involving the innate immune response and TNF
All-sky search for gravitational-wave bursts in the second joint LIGO-Virgo run
- Author
- Abadie J
- Abbott BP
- Abbott R
- Abbott TD
- Abernathy M
- Accadia T
- Acernese F
- Adams C
- Adhikari R
- Affeldt C
- Agathos M
- Agatsuma K
- Ajith P
- Allen B
- Amariutei D
- Anderson SB
- Anderson WG
- Arai K
- Arain MA
- Araya MC
- Aston SM
- Astone P
- Atkinson D
- Aufmuth P
- Aulbert C
- Aylott BE
- Babak S
- Baker P
- Ballardin G
- Ballmer S
- Barayoga JCB
- Barker D
- Barone F
- Barr B
- Barrera C. Oropeza
- Barsotti L
- Barsuglia M
- Barton MA
- Bartos I
- Bassiri R
- Bastarrika M
- Basti A
- Batch J
- Bauchrowitz J
- Bauer TS
- Bebronne M
- Beck D
- Behnke B
- Bejger M
- Beker MG
- Bell AS
- Belletoile A
- Belopolski I
- Benacquista M
- Berliner JM
- Bertolini A
- Betzwieser J
- Beveridge N
- Beyersdorf PT
- Bilenko IA
- Billingsley G
- Birch J
- Biswas R
- Bitossi M
- Bizouard MA
- Black E
- Blackburn JK
- Blackburn L
- Blair D
- Bland B
- Blom M
- Bock O
- Bodiya TP
- Bogan C
- Bondarescu R
- Bondu F
- Bonelli L
- Bonnand R
- Bork R
- Born M
- Boschi V
- Bose S
- Bosi L
- Bouhou B
- Braccini S
- Bradaschia C
- Brady PR
- Braginsky VB
- Branchesi M
- Brau JE
- Breyer J
- Briant T
- Bridges DO
- Brillet A
- Brinkmann M
- Brisson V
- Britzger M
- Brooks AF
- Brown DA
- Bueso X. Portell
- Bulik T
- Bulten HJ
- Buonanno A
- Burguet-Castell J
- Buskulic D
- Buy C
- Byer RL
- Cadonati L
- Cagnoli G
- Calloni E
- Camp JB
- Campsie P
- Cannizzo J
- Cannon K
- Canuel B
- Cao J
- Capano CD
- Carbognani F
- Carbone L
- Caride S
- Caudill S
- Cavaglia M
- Cavalcanti T. Perez
- Cavalier F
- Cavalieri R
- Cella G
- Cepeda C
- Ceron EA
- Cesarini E
- Chaibi O
- Chalermsongsak T
- Charlton P
- Chassande-Mottin E
- Chelkowski S
- Chen W
- Chen X
- Chen Y
- Chincarini A
- Chiummo A
- Cho HS
- Chow J
- Christensen N
- Chua SSY
- Chung CTY
- Chung S
- Ciani G
- Clara F
- Clark DE
- Clark J
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- Cleva F
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- Cohadon PF
- Colacino CN
- Colas J
- Colla A
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- Conte A
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- Coulon JP
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- Coward DM
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- Coyne DC
- Creighton JDE
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- Cunningham L
- Cuoco E
- Cutler RM
- D'Antonio S
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- Damazio D. Oliveira
- Danilishin SL
- Dannenberg R
- Danzmann K
- Dattilo V
- Daudert B
- Daveloza H
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- Daw EJ
- Day R
- Dayanga T
- de Lima J. G. Rocha
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- Debreczeni G
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- Drever RWP
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- Ferrando B. M. Salvachua
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- Publication venue
- 'American Physical Society (APS)'
- Publication date
- 01/01/2012
- Field of study
We present results from a search for gravitational-wave bursts in the data
collected by the LIGO and Virgo detectors between July 7, 2009 and October 20,
2010: data are analyzed when at least two of the three LIGO-Virgo detectors are
in coincident operation, with a total observation time of 207 days. The
analysis searches for transients of duration < 1 s over the frequency band
64-5000 Hz, without other assumptions on the signal waveform, polarization,
direction or occurrence time. All identified events are consistent with the
expected accidental background. We set frequentist upper limits on the rate of
gravitational-wave bursts by combining this search with the previous LIGO-Virgo
search on the data collected between November 2005 and October 2007. The upper
limit on the rate of strong gravitational-wave bursts at the Earth is 1.3
events per year at 90% confidence. We also present upper limits on source rate
density per year and Mpc^3 for sample populations of standard-candle sources.
As in the previous joint run, typical sensitivities of the search in terms of
the root-sum-squared strain amplitude for these waveforms lie in the range 5
10^-22 Hz^-1/2 to 1 10^-20 Hz^-1/2. The combination of the two joint runs
entails the most sensitive all-sky search for generic gravitational-wave bursts
and synthesizes the results achieved by the initial generation of
interferometric detectors.Comment: 15 pages, 7 figures: data for plots and archived public version at
https://dcc.ligo.org/cgi-bin/DocDB/ShowDocument?docid=70814&version=19, see
also the public announcement at
http://www.ligo.org/science/Publication-S6BurstAllSky
Search for the standard model Higgs boson in the diphoton decay channel with 4.9fb -1 of pp collision data at √s=7TeV with atlas
- Author
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- Yacoob S
- Yamada M
- Yamaguchi H
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- Yamamoto K
- Yamamoto S
- Yamamura T
- Yamanaka T
- Yamaoka J
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- Yamazaki Y
- Yan Z
- Yang H
- Yang UK
- Yang Y
- Yang Y
- Yang Z
- Yanush S
- Yao Y
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- Ye J
- Ye S
- Yilmaz M
- Yoosoofmiya R
- Yorita K
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- Youssef S
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- Zajacova Z
- Zanello L
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- Zevi Della Porta G
- Zhan Z
- Zhang D
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- Zhao Z
- Zhemchugov A
- Zheng S
- Zhong J
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- Zhu CG
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- Zhuang X
- Zhuravlov V
- Zieminska D
- Zimmermann R
- Zimmermann S
- Zimmermann S
- Ziolkowski M
- Zitoun R
- Zmouchko VV
- Zobernig G
- Zoccoli A
- Zolnierowski Y
- Zsenei A
- Zur Nedden M
- Zutshi V
- Zwalinski L
- Åkesson TPA
- Åsman B
- Publication venue
- Publication date
- 01/01/2012
- Field of study
A search for the standard model Higgs boson is performed in the diphoton decay channel. The data used correspond to an integrated luminosity of 4.9 fb-1 collected with the ATLAS detector at the Large Hadron Collider in proton-proton collisions at a center-of-mass energy of √s=7 TeV. In the diphoton mass range 110–150 GeV, the largest excess with respect to the background-only hypothesis is observed at 126.5 GeV, with a local significance of 2.8 standard deviations. Taking the look-elsewhere effect into account in the range 110–150 GeV, this significance becomes 1.5 standard deviations. The standard model Higgs boson is excluded at 95% confidence level in the mass ranges of 113–115 GeV and 134.5–136 GeV
Search for the standard model Higgs boson in the diphoton decay channel with 4.9fb -1 of pp collision data at √s=7TeV with atlas
- Author
- Aad G
- Abbott B
- Abdallah J
- Abdel Khalek S
- Abdelalim AA
- Abdesselam A
- Abdinov O
- Abi B
- Abolins M
- Abouzeid OS
- Abramowicz H
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- Acharya BS
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- Akimoto G
- Akimov AV
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- Aleksandrov IN
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- Yamaoka J
- Yamazaki T
- Yamazaki Y
- Yan Z
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- Yang Y
- Yang Y
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- Yanush S
- Yao Y
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- Yilmaz M
- Yoosoofmiya R
- Yorita K
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- Youssef S
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- Zabinski B
- Zaets VG
- Zaidan R
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- Zajacova Z
- Zanello L
- Zaytsev A
- Zeitnitz C
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- Zeman M
- Zemla A
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- Zenin O
- Zenonos Z
- Zenz S
- Zerwas D
- Zevi Della Porta G
- Zhan Z
- Zhang D
- Zhang H
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- Zhao T
- Zhao Z
- Zhemchugov A
- Zheng S
- Zhong J
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- Zhu H
- Zhu J
- Zhu Y
- Zhuang X
- Zhuravlov V
- Zieminska D
- Zimmermann R
- Zimmermann S
- Zimmermann S
- Ziolkowski M
- Zitoun R
- Zmouchko VV
- Zobernig G
- Zoccoli A
- Zolnierowski Y
- Zsenei A
- Zur Nedden M
- Zutshi V
- Zwalinski L
- Åkesson TPA
- Åsman B
- Publication venue
- Publication date
- 01/01/2012
- Field of study
A search for the standard model Higgs boson is performed in the diphoton decay channel. The data used correspond to an integrated luminosity of 4.9 fb-1 collected with the ATLAS detector at the Large Hadron Collider in proton-proton collisions at a center-of-mass energy of √s=7 TeV. In the diphoton mass range 110–150 GeV, the largest excess with respect to the background-only hypothesis is observed at 126.5 GeV, with a local significance of 2.8 standard deviations. Taking the look-elsewhere effect into account in the range 110–150 GeV, this significance becomes 1.5 standard deviations. The standard model Higgs boson is excluded at 95% confidence level in the mass ranges of 113–115 GeV and 134.5–136 GeV
NKG2A complexed with CD94 defines a novel inhibitory natural killer cell receptor
- Publication venue
- 'Rockefeller University Press'
- Publication date
- 17/02/1997
- Field of study
CD94 is a C-type lectin expressed by natural killer (NK) cells and a subset of T cells. Blocking studies using anti-CD94 mAbs have suggested that it is a receptor for human leukocyte antigen class I molecules. CD94 has recently been shown to be a 26-kD protein covalently associated with an unidentified 43-kD protein(s). This report shows that NKG2A, a 43-kD protein, is covalently associated with CD94 on the surface of NK cells. Cell surface expression of NKG2A is dependent on the association with CD94 as glycosylation patterns characteristic of mature proteins are found only in NKG2A that is associated with CD94. Analysis of NK cell clones showed that NKG2A was expressed in all NK cell clones whose CD16-dependent killing was inhibited by cross-linking CD94. The induction of an inhibitory signal is consistent with the presence of two immunoreceptor tyrosine-based inhibitory motifs (V/LXYXXL) on the cytoplasmic domain of NKG2A. Similar motifs are found on Ly49 and killer cell inhibitory receptors, which also transmit negative signals to NK cells
Human Leukocyte Antigen (HLA) Typing by DNA Sequencing
- Author
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
A novel strategy for defining haplotypes by selective depletion using restriction enzymes
- Author
- AG Randolph
- Andrey Morgun
- Anna S. Smirnova
- CA Cuff
- CE Whichelow
- CF Xu
- D Altshuler
- DC Crawford
- DL Wheeler
- F Lamsis
- F Pociot
- G Messer
- GE Nedwin
- JC Knight
- JC Knight
- JC Stephens
- JN Hirschhorn
- JP Feugeas
- Karina L. Mine
- KS Park
- Kátia C. Ferreira-Silva
- M Nagano
- Maria Gerbase-DeLima
- MG Manz
- Natalia Shulzhenko
- O Migita
- PE Posch
- PM Giffard
- RM Salem
- S Gustincich
- Vinicius Andrade-Oliveira
- Y Eitan
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
Inhibition of Human Immunodeficiency Virus Replication by Cell Membrane–Crossing Oligomers
- Author
- A Schick
- Adam Fletcher
- AL Brass
- B Hyrup
- B Urban-Klein
- Birgit Werner
- BM Tyler
- C Bohler
- CA Stein
- Cornelia Lass-Flörl
- CR Jung
- D Lochmann
- D Wilflingseder
- Doris Wilflingseder
- F Steindl
- FMF Chen
- Heribert Stoiber
- Holger Bock
- IR Gilmore
- J Lisziewicz
- J Soutschek
- J Vandesompele
- JJ Turner
- JO McNamara
- JW Park
- M Bennett
- MA Martinez
- MA Robbins
- ML Patil
- PE Nielsen
- PY Lu
- S Agrawal
- S Agrawal
- S Akhtar
- S Sabbioni
- S Sei
- Stefan Piper
- T Koch
- Thomas Lindhorst
- U Schöllkopf
- VV Demidov
- Wilfried Posch
- XF Qin
- Y Suzuki
- YL Chiu
- Publication venue
- ScholarOne
- Publication date
- Field of study
Although rapidly becoming a valuable tool for gene silencing, regulation or editing in vitro, the direct transfer of small interfering ribonucleic acids (siRNAs) into cells is still an unsolved problem for in vivo applications. For the first time, we show that specific modifications of antisense oligomers allow autonomous passage into cell lines and primary cells without further adjuvant or coupling to a cell-penetrating peptide. For this reason, we termed the specifically modified oligonucleotides “cell membrane–crossing oligomers” (CMCOs). CMCOs targeted to various conserved regions of human immunodeficiency virus (HIV)-1 were tested and compared with nontargeting CMCOs. Analyses of uninfected and infected cells incubated with labeled CMCOs revealed that the compounds were enriched in infected cells and some of the tested CMCOs exhibited a potent antiviral effect. Finally, the CMCOs did not exert any cytotoxicity and did not inhibit proliferation of the cells. In vitro, our CMCOs are promising candidates as biologically active anti-HIV reagents for future in vivo applications