<?xml version="1.0" encoding="UTF-8"?><rss xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:content="http://purl.org/rss/1.0/modules/content/" xmlns:atom="http://www.w3.org/2005/Atom" version="2.0"><channel><title><![CDATA[Dan Peer]]></title><description><![CDATA[Dan Peer]]></description><link>https://dmedalion.wixsite.com/dan-peer/blog</link><generator>RSS for Node</generator><lastBuildDate>Tue, 28 Apr 2026 22:51:19 GMT</lastBuildDate><atom:link href="https://danpeerlab.sites.tau.ac.il/blog-feed.xml" rel="self" type="application/rss+xml"/><item><title><![CDATA[Progress and challenges towards targeted delivery of cancer therapeutics]]></title><description><![CDATA[Rosenblum D, Joshi N, Tao W, Karp JM and Peer D Nat Commun (2018) 9;1410, 1-12 Targeted delivery approaches for cancer therapeutics have shown a steep rise over the past few decades. However, compared to the plethora of successful pre-clinical studies, only 15 passively targeted nanocarriers (NCs) have been approved for clinical use and none of the actively targeted NCs have advanced past clinical trials. Herein, we review the principles behind targeted delivery approaches to determine...]]></description><link>https://danpeerlab.sites.tau.ac.il/post/progress-and-challenges-towards-targeted-delivery-of-cancer-therapeutics</link><guid isPermaLink="false">6968dfc5059a56b31bda87ee</guid><category><![CDATA[Reviews]]></category><pubDate>Thu, 15 Jan 2026 12:39:44 GMT</pubDate><enclosure url="https://static.wixstatic.com/media/50b598_ab5ea81311bb4ca38aa45459031fdf66~mv2.jpg/v1/fit/w_566,h_320,al_c,q_80/file.png" length="0" type="image/png"/><dc:creator>Prof. Dan Peer</dc:creator></item><item><title><![CDATA[Special delivery: targeted therapy with small RNAs]]></title><description><![CDATA[Peer D, Lieberman J Gene Ther (2011) 18(12):1127-1133. Harnessing RNA interference using small RNA-based drugs has great potential to develop drugs designed to knock down expression of any disease-causing gene, thereby greatly expanding the universe of possible drug targets. However, delivering small RNAs into specific tissues and cells is still a hurdle. Here, we review recent progress in overcoming systemic, local and cellular barriers to RNA drug delivery, focusing on strategies for...]]></description><link>https://danpeerlab.sites.tau.ac.il/post/special-delivery-targeted-therapy-with-small-rnas</link><guid isPermaLink="false">6968df123e23fce2936f0d15</guid><category><![CDATA[Reviews]]></category><pubDate>Thu, 15 Jan 2026 12:37:36 GMT</pubDate><enclosure url="https://static.wixstatic.com/media/50b598_ca9454437047461dbe05ec01bb61f948~mv2.jpg/v1/fit/w_566,h_320,al_c,q_80/file.png" length="0" type="image/png"/><dc:creator>Prof. Dan Peer</dc:creator></item><item><title><![CDATA[Polysaccharides as building blocks for nanotherapeutics]]></title><description><![CDATA[Mizrahy S and  Peer D Chem Soc Rev. (2012), 41(7):2623-2640. The use of polysaccharides as building blocks in the development of nano-sized drug delivery systems is rapidly growing. This can be attributed to the outstanding virtues of polysaccharides such as biocompatibility, biodegradability, low toxicity and low cost. In addition, the variety of physicochemical properties and the ease of chemical modifications enable the preparation of a wide array of nanoparticles. This tutorial review...]]></description><link>https://danpeerlab.sites.tau.ac.il/post/polysaccharides-as-building-blocks-for-nanotherapeutics</link><guid isPermaLink="false">6968ddfd3e23fce2936f0a19</guid><category><![CDATA[Reviews]]></category><pubDate>Thu, 15 Jan 2026 12:33:11 GMT</pubDate><enclosure url="https://static.wixstatic.com/media/50b598_e592a0f32ba5459cb33ae7bfd21a0f14~mv2.jpg/v1/fit/w_566,h_320,al_c,q_80/file.png" length="0" type="image/png"/><dc:creator>Prof. Dan Peer</dc:creator></item><item><title><![CDATA[Systemic Gene Silencing in Primary T Lymphocytes Using Targeted Lipid Nanoparticles]]></title><description><![CDATA[Ramishetti S, Kedmi R, Goldsmith M, Leonard F, Sprague AG, Godin B, Gozin M, Cullis PR, Dykxhoorn DM, Peer D. ACS Nano (2015) 9(7):6706-6716. Modulating T cell function by down-regulating specific genes using RNA interference (RNAi) holds tremendous potential in advancing targeted therapies in many immune-related disorders including cancer, inflammation, autoimmunity, and viral infections. Hematopoietic cells, in general, and primary T lymphocytes, in particular, are notoriously hard to...]]></description><link>https://danpeerlab.sites.tau.ac.il/post/systemic-gene-silencing-in-primary-t-lymphocytes-using-targeted-lipid-nanoparticles</link><guid isPermaLink="false">6968db79022bfc82f762d910</guid><category><![CDATA[Manuscripts]]></category><pubDate>Thu, 15 Jan 2026 12:22:21 GMT</pubDate><enclosure url="https://static.wixstatic.com/media/50b598_9255721de7b8430195d912fdb73ed634~mv2.jpg/v1/fit/w_566,h_320,al_c,q_80/file.png" length="0" type="image/png"/><dc:creator>Prof. Dan Peer</dc:creator></item><item><title><![CDATA[A modular platform for targeted RNAi therapeutics]]></title><description><![CDATA[Kedmi R, Veiga N, Ramishetti S, Goldsmith M, Rosenblum D, Dammes N, Hazan-Halevy I, Nahary L, Leviatan-Ben-Arye S, Harlev M, Behlke M, Benhar I, Lieberman J, Peer D. (2018) Previous studies have identified relevant genes and signaling pathways that are hampered in human disorders as potential candidates for therapeutics. Developing nucleic acid-based tools to manipulate gene expression, such as short interfering RNAs (siRNAs), opens up opportunities for personalized medicine. Yet, although...]]></description><link>https://danpeerlab.sites.tau.ac.il/post/a-modular-platform-for-targeted-rnai-therapeutics</link><guid isPermaLink="false">6968db1844e01db33afdc10c</guid><category><![CDATA[Manuscripts]]></category><pubDate>Thu, 15 Jan 2026 12:19:41 GMT</pubDate><enclosure url="https://static.wixstatic.com/media/50b598_37d190cb74174eda92cd83b5a55b1c1f~mv2.jpg/v1/fit/w_566,h_320,al_c,q_80/file.png" length="0" type="image/png"/><dc:creator>Prof. Dan Peer</dc:creator></item><item><title><![CDATA[Cell specific delivery of modified mRNA expressing therapeutic proteins to leukocytes]]></title><description><![CDATA[Veiga N, Goldsmith M, Granot Y, Rosenblum D, Dammes N, Kedmi R, Ramishetti S, Peer D. (2018) Therapeutic alteration of gene expression in vivo can be achieved by delivering nucleic acids (e.g., mRNA, siRNA) using nanoparticles. Recent progress in modified messenger RNA (mmRNA) synthesis facilitated the development of lipid nanoparticles (LNPs) loaded with mmRNA as a promising tool for in vivo protein expression. Although progress have been made with mmRNA-LNPs based protein expression in...]]></description><link>https://danpeerlab.sites.tau.ac.il/post/cell-specific-delivery-of-modified-mrna-expressing-therapeutic-proteins-to-leukocytes</link><guid isPermaLink="false">6968d9b8059a56b31bda75fd</guid><category><![CDATA[Manuscripts]]></category><pubDate>Thu, 15 Jan 2026 12:17:40 GMT</pubDate><enclosure url="https://static.wixstatic.com/media/50b598_846563530a324644a40af789b865584b~mv2.jpg/v1/fit/w_566,h_320,al_c,q_80/file.png" length="0" type="image/png"/><dc:creator>Prof. Dan Peer</dc:creator></item><item><title><![CDATA[Colon Targeting by Lipid Nanoparticles as a Platform for mRNA Therapeutics]]></title><description><![CDATA[A new LNPs (30-n-LNPs) formulation with increasing phospholipids is investigated as a possible mRNA delivery system for treating Inflammatory Bowel Diseases. Compared to LNPs with benchmark composition (b-LNPs), n-LNPs containing 30% distearoylphosphatidylcholine (DSPC) are well tolerated following intravenous administration and display natural targeting toward the inflamed colon in dextran sodium sulfate (DSS)-colitis bearing mice, while de-targeting clearing organs such as the liver and...]]></description><link>https://danpeerlab.sites.tau.ac.il/post/colon-targeting-by-lipid-nanoparticles-as-a-platform-for-mrna-therapeutics</link><guid isPermaLink="false">696801b50ef3e0e1c07f31ab</guid><category><![CDATA[Research]]></category><pubDate>Wed, 14 Jan 2026 20:51:42 GMT</pubDate><enclosure url="https://static.wixstatic.com/media/50b598_82eb0cae608643a28eb2e5a1bda32dbd~mv2.jpg/v1/fit/w_1000,h_1000,al_c,q_80/file.png" length="0" type="image/png"/><dc:creator>Prof. Dan Peer</dc:creator></item><item><title><![CDATA[mRNA-LNP Vaccine Provides Protection Against Bacterium]]></title><description><![CDATA[Messenger RNA (mRNA) lipid nanoparticle (LNP) vaccines have emerged as an effective vaccination strategy. Although currently applied toward viral pathogens, data concerning the platform’s effectiveness against bacterial pathogens are limited. Here, we developed an effective mRNA-LNP vaccine against a lethal bacterial pathogen by optimizing mRNA payload guanine and cytosine content and antigen design. We designed a nucleoside-modified mRNA-LNP vaccine based on the bacterial F1 capsule antigen,...]]></description><link>https://danpeerlab.sites.tau.ac.il/post/mrna-lnp-vaccine-provides-protection-against-bacterium</link><guid isPermaLink="false">696801476ae8988b73fb6826</guid><category><![CDATA[Research]]></category><pubDate>Wed, 14 Jan 2026 20:50:29 GMT</pubDate><enclosure url="https://static.wixstatic.com/media/50b598_76cbbb6995d34f5f9712798f6df0f7eb~mv2.jpg/v1/fit/w_640,h_400,al_c,q_80/file.png" length="0" type="image/png"/><dc:creator>Prof. Dan Peer</dc:creator></item><item><title><![CDATA[ERC Project: Circular RNA Therapeutics for Duchenne Muscular Dystrophy]]></title><description><![CDATA[RNA therapeutics is an emerging field explored in various types of diseases such as genetic disorders, cancer, inflammation and viral infections. Currently, most of the research focuses on the delivery of mRNA molecules that will transiently express a certain protein that can replace a defective protein or manipulate gene expression in the cells. My lab was the first to show systemic, cell-specific delivery of mRNA molecules in animals. Our approach was translated to several clinical trials...]]></description><link>https://danpeerlab.sites.tau.ac.il/post/erc-project-circular-rna-therapeutics-for-duchenne-muscular-dystrophy</link><guid isPermaLink="false">6968010b14d81ccd4b53820c</guid><category><![CDATA[Research]]></category><pubDate>Wed, 14 Jan 2026 20:48:39 GMT</pubDate><enclosure url="https://static.wixstatic.com/media/50b598_4ad767cb7899411bb9999f08fe4598c3~mv2.jpeg/v1/fit/w_252,h_200,al_c,q_80/file.png" length="0" type="image/png"/><dc:creator>Prof. Dan Peer</dc:creator></item><item><title><![CDATA[Conformation-sensitive targeting of lipid nanoparticles for RNA therapeutics]]></title><description><![CDATA[We use a conformation-sensitive targeting strategy to achieve in vivo gene silencing in a selective subset of leukocytes and show potential therapeutic applications in a murine model of colitis. In particular, by targeting the high-affinity conformation of α4β7 integrin, which is a hallmark of inflammatory gut-homing leukocytes, we silenced interferon-γ in the gut, resulting in an improved therapeutic outcome in experimental colitis. The lipid nanoparticles did not induce adverse immune...]]></description><link>https://danpeerlab.sites.tau.ac.il/post/conformation-sensitive-targeting-of-lipid-nanoparticles-for-rna-therapeutics</link><guid isPermaLink="false">696800cb0ef3e0e1c07f2f5d</guid><category><![CDATA[Research]]></category><pubDate>Wed, 14 Jan 2026 20:47:36 GMT</pubDate><enclosure url="https://static.wixstatic.com/media/50b598_f018e40b460c4a60858c0d9eaa243e1f~mv2.jpg/v1/fit/w_640,h_400,al_c,q_80/file.png" length="0" type="image/png"/><dc:creator>Prof. Dan Peer</dc:creator></item><item><title><![CDATA[Genome editing approaches for in vivo gene therapy]]></title><description><![CDATA[Genome editing approaches such as CRISPR/Cas9 system is routinely used to permanently and precisely disrupt potentially any gene of interest. Yet the efficiency of gene editing is still low. Recently we developed a safe and efficient lipid-nanoparticle (LNP) for the delivery of Cas9 mRNA and sgRNAs that utilize our novel amino-ionizable lipid for high-efficiency therapeutic genome editing in aggressive cancer. We plan to expand this line of research to other types of diseases such as rare...]]></description><link>https://danpeerlab.sites.tau.ac.il/post/genome-editing-approaches-for-in-vivo-gene-therapy</link><guid isPermaLink="false">6968004614d81ccd4b537ffd</guid><category><![CDATA[Research]]></category><pubDate>Wed, 14 Jan 2026 20:45:45 GMT</pubDate><enclosure url="https://static.wixstatic.com/media/50b598_c7a703dd2e7d48e3aff3f89f42963ee1~mv2.jpg/v1/fit/w_566,h_320,al_c,q_80/file.png" length="0" type="image/png"/><dc:creator>Prof. Dan Peer</dc:creator></item><item><title><![CDATA[RNAs vaccines (mRNA, cirRNA, and saRNA)]]></title><description><![CDATA[RNA vaccines work by introducing an mRNA sequence, which is coded for a disease-specific antigen. This antigen is recognized by the immune system and starts an immune (cellular and humoral) response. Our lab is being involved in developing different types of mRNA vaccines for outbreaks such as Coronaviruses and sessional flu utilizing our novel, fully degradable amino ionizable lipids. Uri Elia et al  (2021)  Design of SARS-CoV2 hFc-Conjugated Receptor-Binding Domain mRNA Vaccine Delivered...]]></description><link>https://danpeerlab.sites.tau.ac.il/post/rnas-vaccines-mrna-cirrna-and-sarna</link><guid isPermaLink="false">6967ffd114d81ccd4b537ecc</guid><category><![CDATA[Research]]></category><pubDate>Wed, 14 Jan 2026 20:44:19 GMT</pubDate><enclosure url="https://static.wixstatic.com/media/50b598_04088d99919f493c936ff544d9f2216c~mv2.jpg/v1/fit/w_1000,h_855,al_c,q_80/file.png" length="0" type="image/png"/><dc:creator>Prof. Dan Peer</dc:creator></item><item><title><![CDATA[Utilizing RNAs for in vivo drug discovery]]></title><description><![CDATA[We are harnessing RNA payloads (RNAi, mRNA, saRNA, and cirRNA)  as in vivo tools for drug discovery. Nucleic acids loaded lipid nanoparticles have emerged as a promising therapeutic approach for various malignancies, rare genetic diseases, and inflammation. We aim to utilize RNA-loaded lipid nanoparticles to identify in vivo (in their biological environment) new potential drug targets that could be then applied to therapeutics in various malignancies, including head &#38; neck cancer,...]]></description><link>https://danpeerlab.sites.tau.ac.il/post/utilizing-rnas-for-in-vivo-drug-discovery</link><guid isPermaLink="false">6967ff51801fea0f88097f57</guid><category><![CDATA[Research]]></category><pubDate>Wed, 14 Jan 2026 20:42:21 GMT</pubDate><enclosure url="https://static.wixstatic.com/media/50b598_3c4a9ec9eb4748b7bcebbc8f92c4176a~mv2.jpg/v1/fit/w_1000,h_1000,al_c,q_80/file.png" length="0" type="image/png"/><dc:creator>Prof. Dan Peer</dc:creator></item><item><title><![CDATA[Studying novel approaches to target tumor cells]]></title><description><![CDATA[This research was initiated in order to manipulate adult stem cells in vivo using nucleic acids-based targeted therapeutics.]]></description><link>https://danpeerlab.sites.tau.ac.il/post/studying-novel-approaches-to-target-tumor-cells</link><guid isPermaLink="false">6967ff160ef3e0e1c07f2ae5</guid><category><![CDATA[Research]]></category><pubDate>Wed, 14 Jan 2026 20:40:14 GMT</pubDate><enclosure url="https://static.wixstatic.com/media/50b598_12fd7aef00f84975aebb1b1dbee24166~mv2.jpg/v1/fit/w_566,h_320,al_c,q_80/file.png" length="0" type="image/png"/><dc:creator>Prof. Dan Peer</dc:creator></item><item><title><![CDATA[Designing novel therapeutic strategies for hematological malignancies]]></title><description><![CDATA[This research aims to develop novel nucleic acids-based therapeutics for hematological malignancies.]]></description><link>https://danpeerlab.sites.tau.ac.il/post/designing-novel-therapeutic-strategies-for-hematological-malignancies</link><guid isPermaLink="false">6967fe0814d81ccd4b5379cf</guid><category><![CDATA[Research]]></category><pubDate>Wed, 14 Jan 2026 20:39:17 GMT</pubDate><enclosure url="https://static.wixstatic.com/media/50b598_b566151f699b442eba972ac30e284373~mv2.jpg/v1/fit/w_566,h_320,al_c,q_80/file.png" length="0" type="image/png"/><dc:creator>Prof. Dan Peer</dc:creator></item><item><title><![CDATA[Breaching the BBB to deliver therapies into the CNS]]></title><description><![CDATA[The focus of this research is to design novel neurotrophic virus inspired nanotherapeutics to deliver nucleic acids into the CNS. We aim to utilize such therapeutic modality and develop new remedies for neurodevelopmental disorders.]]></description><link>https://danpeerlab.sites.tau.ac.il/post/breaching-the-bbb-to-deliver-therapies-into-the-cns</link><guid isPermaLink="false">6967fd5c14d81ccd4b5377d5</guid><category><![CDATA[Research]]></category><pubDate>Wed, 14 Jan 2026 20:33:45 GMT</pubDate><enclosure url="https://static.wixstatic.com/media/50b598_bd9790e36540482696c05c6c35b403c0~mv2.png/v1/fit/w_565,h_318,al_c,q_80/file.png" length="0" type="image/png"/><dc:creator>Prof. Dan Peer</dc:creator></item><item><title><![CDATA[Probing and manipulating the immune system with nanoparticles]]></title><description><![CDATA[We aspire to utilize oligonucleotides loaded LNPs for in vivo reprograming of leukocytes and thus to design novel immunomodulatory therapeutic approaches for autoimmune disorders and cancer.]]></description><link>https://danpeerlab.sites.tau.ac.il/post/probing-and-manipulating-the-immune-system-with-nanoparticles</link><guid isPermaLink="false">6967fd3814d81ccd4b53777e</guid><category><![CDATA[Research]]></category><pubDate>Wed, 14 Jan 2026 20:32:07 GMT</pubDate><enclosure url="https://static.wixstatic.com/media/50b598_55a0131b82ef4d53822bec9b93674916~mv2.jpg/v1/fit/w_566,h_320,al_c,q_80/file.png" length="0" type="image/png"/><dc:creator>Prof. Dan Peer</dc:creator></item><item><title><![CDATA[Investigating novel cancer multidrug resistance inhibitors]]></title><description><![CDATA[The goal of this project is to explore resistance pathways of cancer cells and translate the acquired knowledge by designing novel RNAi-based nanotherapeutics.]]></description><link>https://danpeerlab.sites.tau.ac.il/post/investigating-novel-cancer-multidrug-resistance-inhibitors</link><guid isPermaLink="false">6967fcda0d9b34c9e2928770</guid><category><![CDATA[Research]]></category><pubDate>Wed, 14 Jan 2026 20:31:11 GMT</pubDate><enclosure url="https://static.wixstatic.com/media/50b598_2219346abc1b4a198ba9491bb56a5641~mv2.jpg/v1/fit/w_566,h_320,al_c,q_80/file.png" length="0" type="image/png"/><dc:creator>Prof. Dan Peer</dc:creator></item><item><title><![CDATA[Harnessing RNAi as a tool for drug discovery and therapeutic applications]]></title><description><![CDATA[We aim to utilize RNA-loaded lipid nanoparticles in order to design new therapeutic modalities for various malignancies, including head &#38; neck cancer, glioblastoma and breast cancer.]]></description><link>https://danpeerlab.sites.tau.ac.il/post/harnessing-rnai-as-a-tool-for-drug-discovery-and-therapeutic-applications</link><guid isPermaLink="false">6967fc52801fea0f88097704</guid><category><![CDATA[Research]]></category><pubDate>Wed, 14 Jan 2026 20:29:37 GMT</pubDate><enclosure url="https://static.wixstatic.com/media/50b598_f18ac86b6d714a9bbf005420052afe09~mv2.jpg/v1/fit/w_566,h_320,al_c,q_80/file.png" length="0" type="image/png"/><dc:creator>Prof. Dan Peer</dc:creator></item><item><title><![CDATA[Developing novel strategies for targeted drug delivery]]></title><description><![CDATA[We aim to design novel platforms for a selective delivery of therapeutic payload to specific target cells, thus increasing the efficiency and reducing adverse effects.]]></description><link>https://danpeerlab.sites.tau.ac.il/post/developing-novel-strategies-for-targeted-drug-delivery</link><guid isPermaLink="false">6967fbff0d9b34c9e292852f</guid><category><![CDATA[Research]]></category><pubDate>Wed, 14 Jan 2026 20:27:20 GMT</pubDate><enclosure url="https://static.wixstatic.com/media/50b598_033475b086b14b74b97a5afc2bb373ea~mv2.jpg/v1/fit/w_566,h_320,al_c,q_80/file.png" length="0" type="image/png"/><dc:creator>Prof. Dan Peer</dc:creator></item></channel></rss>