Author Information

Is this project an undergraduate, graduate, or faculty project?

Undergraduate

Project Type

individual

Campus

Daytona Beach

Authors' Class Standing

Leia Spaniak, Senior

Lead Presenter's Name

Leia Spaniak

Lead Presenter's College

DB College of Engineering

Faculty Mentor Name

Cagri Kilic

Abstract

The purpose of this research is to investigate how a biological immune-based response can be employed to create a self-evolving cybersecurity framework for aerospace navigation systems. Specifically, as part of Project SENTINEL, this research identifies key members of dendritic cells (DCs) to understand their mechanisms for detecting diverse varieties of foreign invaders, from malignant bacteria to viral infections. The multi-layered approach of Pathogen Recognition Receptors (PRRs) in threat detection contributes to the innate immune system by employing a diverse array of generalized and specialized receptors, such as varieties of Toll-Like Receptors (TLRs) and Nod-Like Receptors (NLRs), which can trigger inflammatory responses. This process provides guidance for detecting new threats or Advanced Persistent Threats (APTs) in a security framework, particularly through sensor attack detection. B-cells and T-cells contribute to the adaptive response by first employing non-specific naïve B-cell receptors, which require confirmation from T cells to activate immune responses. Once activated, these cells differentiate into memory B cells, which no longer rely on substantial assistance from T cells to produce specialized antibodies. This research aims to investigate specific AI/ML methods based on these immune system mechanisms to enhance the detection of novel attacks and threat detection response adaptation.

Did this research project receive funding support (Spark, SURF, Research Abroad, Student Internal Grants, Collaborative, Climbing, or Ignite Grants) from the Office of Undergraduate Research?

No

Share

COinS
 

Bio-Inspired Cybersecurity: Adapting Immune System Strategies for Threat Detection in Autonomous Aerospace Navigation

The purpose of this research is to investigate how a biological immune-based response can be employed to create a self-evolving cybersecurity framework for aerospace navigation systems. Specifically, as part of Project SENTINEL, this research identifies key members of dendritic cells (DCs) to understand their mechanisms for detecting diverse varieties of foreign invaders, from malignant bacteria to viral infections. The multi-layered approach of Pathogen Recognition Receptors (PRRs) in threat detection contributes to the innate immune system by employing a diverse array of generalized and specialized receptors, such as varieties of Toll-Like Receptors (TLRs) and Nod-Like Receptors (NLRs), which can trigger inflammatory responses. This process provides guidance for detecting new threats or Advanced Persistent Threats (APTs) in a security framework, particularly through sensor attack detection. B-cells and T-cells contribute to the adaptive response by first employing non-specific naïve B-cell receptors, which require confirmation from T cells to activate immune responses. Once activated, these cells differentiate into memory B cells, which no longer rely on substantial assistance from T cells to produce specialized antibodies. This research aims to investigate specific AI/ML methods based on these immune system mechanisms to enhance the detection of novel attacks and threat detection response adaptation.

 

To view the content in your browser, please download Adobe Reader or, alternately,
you may Download the file to your hard drive.

NOTE: The latest versions of Adobe Reader do not support viewing PDF files within Firefox on Mac OS and if you are using a modern (Intel) Mac, there is no official plugin for viewing PDF files within the browser window.